On July 20, 2022, Health Canada published the Regulations Amending the Food and Drug Regulations (Nutrition Symbols, Other Labelling Provisions, Vitamin D and Hydrogenated Fats or Oils) in the Canada Gazette, Part II (CGII). These regulations amend the Food and Drug Regulations (FDR) to add a new requirement for front-of-package (FOP) nutrition symbol labelling (FOP labelling) for most prepackaged products containing nutrients of public health concern (saturated fat, sugars and/or sodium) at or above specified thresholds. The FOP nutrition symbol (the symbol) will help Canadians to more easily identify foods high in these nutrients. Avoiding excess consumption of these nutrients can help reduce associated health risks.
1.2 About this document
This guide is intended for stakeholders in the Canadian food industry. This includes Canadian manufacturers, retailers and importers of foods for sale in Canada and foreign companies who export food to Canada. The guide provides the Government of Canada's interpretation of the new regulations related to FOP labelling that came into force on July 20, 2022. It is intended to help regulated parties become familiar with core elements of the regulations. The user is encouraged to consult the regulations including Schedule K.1, the Directory of Nutrition Symbol Specifications, the Compendium of Nutrition Symbol Formats, the Table of Daily Values, the Table of Reference Amounts, and the Table of Permitted Nutrient Content Statements and Claims while using this guide.
While this guide provides interpretation of core elements of the symbol requirements, at the end of the transition period, the Canadian Food Inspection Agency's Industry Labelling Tool (ILT) will be updated with guidance on other components of the Regulations Amending the Food and Drug Regulations (Nutrition Symbols, Other Labelling Provisions, Vitamin D and Hydrogenated Fats or Oils) not covered in this guide, such as the addition of vitamin D to milks and margarine and the labelling requirements for foods containing high-intensity sweeteners.
1.3 Disclaimer
This is not a legal document. It is not intended to be used as legal advice about the requirements for FOP labelling as set out in the FDR. The user is encouraged to consult the official version of the applicable legislation and regulations in the Food and Drugs Act and FDR for the purposes of interpreting and applying the law.
The words "prepackaged product", "product" and "food" are used interchangeably throughout this document as are "principal display panel" and "label".
The images used in this guide are not to scale and are for illustrative purposes only. The nutrition symbols are not proportional to the principal display surface (PDS) of the mock-ups.
1.4 Send us your feedback
Health Canada is committed to providing all stakeholders with timely, accurate and reliable information. This includes providing information needed to comply with the requirements for FOP labelling as set out in the FDR. We would appreciate receiving your feedback on whether this guide was useful, and we welcome your suggestions for improvement. Email your feedback to nut.labelling-etiquetage@hc-sc.gc.ca and indicate in the subject line Feedback on the FOP nutrition symbol labelling guide.
2. Overview of the front-of-package (FOP) nutrition symbol labelling rules
The rules for FOP nutrition symbol labelling (FOP labelling) consist of four major parts, which are explained in this guide:
Prohibitions from carrying the FOP nutrition symbol (the symbol)
Nutrient thresholds for the symbol
Exemptions from carrying the symbol
Presentation of the symbol
2.1 When do the regulations come into force?
These regulations came into force on the date they were published in the Canada Gazette, Part II on July 20, 2022. The amendments related to FOP labelling, nutrient content claims, vitamin D fortification and high-intensity sweetener labelling are subject to a transition period that ends December 31, 2025. The transitional provisions for the different components of these amendments are independent of one another. This means that implementation of any requirement within a component (for example, applying the new high-intensity sweetener labelling requirements to prepackaged cookies that contain aspartame) during the transition period will trigger implementation of all requirements within that component but will not trigger implementation of requirements in other components (for example, FOP labelling). Regulated parties must comply with the requirements for all components of these amendments as of January 1, 2026. As of January 1, 2026, information presented in accordance with the former requirements will no longer be compliant. However, products imported, manufactured in Canada or packaged at retail before January 1, 2026 can remain in the warehouse and continue to be sold on store shelves.
2.2 Which foods are subject to the new FOP labelling rules?
The Food and Drug Regulations (FDR) state that the symbol is mandatory for most prepackaged foods sold in Canada, including those manufactured in Canada or imported for sale in Canada. When the symbol is required on a food label, it must be presented in the manner described in the FDR. These requirements are outlined in the Presentation section.
Certain foods or types of foods hold either prohibitions or exemptions from displaying the symbol. The symbol may be voluntarily displayed on labels of foods that have an exemption; however, when it is displayed, the symbol must be presented in the manner described in the FDR.
2.3 How will the regulations be enforced?
While it is Health Canada that develops regulations pertaining to FOP labelling, it is the Canadian Food Inspection Agency (CFIA) that is responsible for the enforcement of the regulations. Health Canada and the CFIA have developed an implementation plan for the transition period. This plan outlines CFIA's compliance and enforcement approach during the transition period.
2.4 Where can I submit my questions?
Health Canada and the CFIA share the responsibility for answering enquiries on the new regulations. Questions on the new requirements and their intent can be submitted to Health Canada at nut.labelling-etiquetage@hc-sc.gc.ca. For questions dealing with compliance and enforcement activities, please refer to the implementation plan on the CFIA website.
3. Foods prohibited from displaying the front-of-package (FOP) nutrition symbol
3.1 Are any foods prohibited from displaying the FOP nutrition symbol?
Yes. The following foods are prohibited from carrying the symbol on their label:
Products intended solely for infants six months of age or older but less than one year of age
Human milk fortifiers
Human milk substitutes (infant formula)
Foods represented as containing a human milk substitute
Formulated liquid diets as defined in section B.24.001 of the Food and Drug Regulations (FDR)
Meal replacements
Nutritional supplements
Foods represented for protein-restricted diets
Foods represented for low (naming the amino acid) diets
Foods represented for use in a very low energy diet as defined in section B.24.001 of the FDR
Reference: subsection B.01.350(15), FDR
4. Nutrient thresholds for the front-of-package (FOP) nutrition symbol
The Food and Drug Regulations (FDR) require that a nutrition symbol appear on the label (specifically, on the principal display panel (PDP)) of a prepackaged product when the amount of saturated fat, sugars and/or sodium is equal to or higher than the specified nutrient thresholds. The regulations specify the thresholds and the approach for determining whether the amount of one or more of these nutrients meets or exceeds them.
Reference: subsections B.01.350(1) to (4), FDR
4.1 What are the FOP nutrition symbol thresholds based on?
The thresholds for the FOP nutrition symbol (the symbol) are based on Daily Values (DVs). For some nutrients, such as fibre, potassium and calcium, the DV is the recommended amount that people in a specific age group should try to consume each day. For other nutrients, such as saturated fat, sugars and sodium, the DV is the amount that people should try not to exceed. The thresholds for the symbol are expressed as percentages of the DV (% DV).
The DVs are found in the Table of Daily Values, which is incorporated by reference into the FDR and available on the Government of Canada website.
4.2 What % DV triggers the FOP nutrition symbol?
For most prepackaged products, a symbol must appear on the label when the amount of saturated fat, sugars and/or sodium is ≥ (equal to or greater than) 15% of the applicable DV set out in column 2 or column 3 of Part 1 of the Table of Daily Values. The DVs in column 2 are the basis of the thresholds for foods intended solely for children one year of age or older but less than four years of age (children one to four years only). The DVs in column 3 are the basis of the thresholds for foods intended for children one to four years of age, or for children four years of age or older and adults (children and/or adults). This is the default requirement.
However, there are two exceptions:
For prepackaged products with a reference amount ≤ (equal to or less than) 30 g or 30 mL, the symbol must appear when the amount of saturated fat, sugars and/or sodium is ≥ 10% of the applicable DV
For prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults), the symbol must appear when the amount of saturated fat, sugars and/or sodium is ≥ 30% of the applicable DV.
Reference: table to section B.01.350, FDR
Table 4.1. Thresholds for the FOP nutrition symbol
Saturated fat
Sugars
Sodium
Prepackaged foods with a reference amount > 30 g or 30 mL that are not main dishes
Prepackaged foods with a reference amount ≤ 30 g or 30 mL
≥ 10% DV
Prepackaged main dishes with a reference amount ≥ 200 g or 170 gFootnote 2
≥ 30% DV
1
Based on the Daily Values (DVs) set out in column 2 of Part 1 of the Table of Daily Values when the product is intended solely for children one to four years and in column 3 when the product is intended for children and/or adults. The % DV threshold for the "high in sat fat" symbol is based on the DV for the sum of saturated fatty acids and trans fatty acids and the % DV must be calculated using only the saturated fat content of the food. Trans fat content is not included.
The Table of Daily Values includes a DV for the sum of saturated fatty acids and trans fatty acids. There is no DV for saturated fat only. The % DV threshold for the "high in sat fat" symbol is based on the DV for the sum of saturated fatty acids and trans fatty acids and the % DV must be calculated using only the saturated fat content of the food. This differs from how to calculate the % DV for saturated fat and trans fat declared in the Nutrition Facts table (NFt). The % DV declared in the NFt must be calculated using the saturated fat and trans fat content combined.
% DV calculated for FOP labelling purposes: (saturated fat content per serving size or reference amount, whichever is greater / DV for the sum of saturated fatty acids and trans fatty acids) x 100
% DV calculated for NFt labelling purposes: (saturated fat and trans fat content combined per serving size / DV for the sum of saturated fatty acids and trans fatty acids) x 100
4.3 What quantity of a food must be used as the basis for determining whether the amount of saturated fat, sugars and/or sodium meets or exceeds the symbol threshold?
In order to determine whether a symbol is required, the amount of saturated fat, sugars and/or sodium in a specific quantity of a food must be assessed against the applicable % DV threshold. That quantity of food is either the serving of stated size (serving size) or the reference amount for the product, whichever quantity is greater.
Reference: subsection B.01.350(2), FDR
There are no prescribed rounding rules for determining whether the nutrient content meets or exceeds the applicable thresholds. However, regulated parties should apply rounding rules that exist for calculating the % DV declared in the NFt.
4.4 What % DV threshold applies to prepackaged products with a reference amount ≤ 30 g or 30 mL whose serving size is larger than the reference amount?
The 10% DV threshold always applies to a product with a small reference amount (more specifically, ≤ 30 g or 30 mL), even when the serving size is larger than 30 g or 30 mL and must be used as the basis when assessing the amount of saturated fat, sugars and/or sodium to determine if a symbol is required. For example, consider a dried meat, such as beef jerky, with a reference amount of 30 g and a serving size of 45 g. Given that the reference amount is 30 g, the applicable threshold is 10% DV. Given that the serving size of 45 g is greater than the reference amount, it must be used as the basis when assessing the amount of saturated fat, sugars and/or sodium against the 10% DV threshold.
5. Foods exempt from the front-of-package (FOP) nutrition symbol requirements
5.1 Are any foods exempt?
Yes, some foods are exempt from the FOP nutrition symbol requirements. An exemption means that a symbol is not required even if the product's saturated fat, sugars and/or sodium content meets or exceeds the applicable threshold, as described in the Thresholds section.
There are two types of exemptions: full exemptions and conditional exemptions.
The products in the following list are always exempt from the FOP requirement. In other words, they are always exempt from the need to assess the saturated fat, sugars and sodium content against the appropriate threshold and therefore they are never required to carry the symbol even if the nutrient content meets or exceeds the threshold. This is known as a full exemption.
Shipping containers, if the container and its contents are not sold as a single unit to a consumer at retail
Examples: a 4 kg box of frozen chicken strips to be served in a cafeteria; a large bag of mixed nuts to be repackaged from bulk by the retailer into smaller amounts; deli meat chubs (whole, not sliced) sold to retailers for the purpose of resale directly by a clerk at the time of sale, from bulk into consumer-sized portions; a shipping container that is destined for retailers who will remove units of fully-labelled consumer prepackaged foods from the container to display them for sale; and a box of six 1.8 kg packages of alfredo sauce to be served in a restaurant.
However, if a shipping container and its contents are sold as a single unit to a consumer at retail the shipping container is subject to the FOP labelling requirements. This includes examples such as a box of 6 x 948 mL tetra packs of chicken broth and 24 x 300 mL bottles of apple juice in shrink wrap that are sold as single units at the retail level.
Products with an available display surface < (less than) 15 cm2
Examples: one-bite confections such as wrapped hard candies, caramels, mints, individual sticks of gum or balls of bubble gum
Individual portions of food that are intended solely to be served by a restaurant or other commercial enterprise with meals or snacks
Examples: individually portioned crackers served with soup and creamers served with a cup of coffee
Ready-to-serve multiple-serving products intended only to be served in a commercial or industrial enterprise or an institution
Examples: frozen, pre-cooked lasagna; gravy; cooked seasoned fish fillets; fresh pasta; pasta sauce; fruit pies; bagels; breakfast cereals; jam; sliced processed meats; and condiments and salad dressings
Products intended only to be used as ingredients in other prepackaged products intended to be sold to consumers at retail or as ingredients in the preparation of food by a commercial or industrial enterprise or an institution
Examples: unbaked lasagna noodles; raw seasoned fish fillets; dried pasta noodles; frozen fries; unbaked fruit pies; canned pie filling; instant potato flakes; dried soup mix; and corn starch
Whole, partly skimmed and skimmed cow or goat's milk sold in refillable glass containers, flavoured whole, partly skimmed and skimmed cow's milk sold in refillable containers as well as cream sold in refillable glass containers
Sweetening agents, including those listed in Division 18 of the Food and Drug Regulations (FDR) and sold as such
Examples: sugar; agave syrup; corn syrup; maple syrup, table syrup; honey; and molasses
Salt and seasoning salt that includes "salt" in its common name and sold as such
Examples: table salt; celery salt; garlic salt; and onion salt
Fats and oils referred to in Division 9 of the FDR, fish and other marine fats and oils, butter, ghee, margarine and other similar substitutes for butter and sold as such
Examples: brick of butter; tub of margarine; bottle of coconut oil; and bottle of canola oil
Individual rations intended for use by military personnel engaged in operations or exercises
Reference: subsection B.01.350(5), FDR
5.3 Which foods have a conditional exemption?
Some products have a conditional exemption from the nutrition symbol requirements. In other words, specific conditions trigger the need to assess the saturated fat, sugars and/or sodium content of the product against the appropriate threshold to determine whether a symbol is required. Losing a conditional exemption does not necessarily mean a product will display the nutrition symbol. The symbol is required on the label only if the content of one or more of these nutrients meets or exceeds the threshold.
For some products, the conditional exemption is based on their conditional exemption from the NFt requirement and for other products it is nutrient-specific based on their ingredients.
5.3.1 Conditional exemption associated with the NFt
The following prepackaged products are conditionally exempt from the symbol requirements when they are also conditionally exempt from carrying an NFt:
Beverages with an alcohol content > (greater than) 0.5%
Raw single ingredient meat, meat by-products, poultry meat or poultry meat by-products that are not ground
Raw single ingredient meat, meat by-products, poultry meat or poultry meat by-products that are ground are always required to carry the NFt, however, they are conditionally exempt from the FOP requirement
Raw single ingredient fish or seafood products
Products sold only in the retail establishment where they are prepared and processed from their ingredients, including from a pre-mix to which an ingredient other than water is added during preparation or processing
Products sold only at road-side stands, craft shows, flea markets, fairs, farmers' markets or sugar bushes by the individual who prepared or processed the products
Individual servings of products sold for immediate consumption and that have not been subjected to a process to extend their durable life, including special packaging
Products sold only in the retail establishment where they are packaged, if they are labelled with a sticker and have an available display surface < 200 cm2
Products that have an available display surface < 100 cm2
Reference: subsection B.01.350(13), FDR
Loss of conditional exemption: As stated above, except for ground meat, meat by-products, poultry meat or poultry meat by-products, the products lose their exemption from the symbol requirements if they lose their exemption from the NFt requirement. The products lose their exemption from carrying an NFt if any of the triggers listed in subsection B.01.401(3) or section B.01.467 of the FDR are present. Ground meat, meat by-products, poultry meat or poultry meat by-products lose their exemption from the FOP requirement if any of the triggers listed in paragraphs B.01.401(3)(a), (b) or (e) are present. For more information, refer to Foods usually exempt from carrying a Nutrition Facts table on the Canadian Food Inspection Agency's (CFIA) Industry Labelling tool.
However, if regulated parties choose to voluntarily display an NFt on one of these otherwise exempt products, the product still maintains its conditional exemption from the symbol requirements.
Reference: subsection B.01.350(13.01), FDR
5.3.2 Nutrient-specific conditional exemption associated with ingredients
For the types of prepackaged products exempt under subsections B.01.350(6) to (12), the conditional nature of the nutrient-specific exemption means that naturally occurring saturated fat, sugars and/or sodium does not trigger the need to assess whether the level of these nutrients meets or exceeds the threshold for the symbol.
5.3.2.1 Foods with health protection benefits
The types of prepackaged products in the following list are conditionally exempt from the symbol requirements, whether standardized or unstandardized, unless otherwise stated:
Whole or cut fresh, frozen, canned or dried fruits or vegetables
Examples of eligible products: chopped, diced, grated, riced and shredded forms of fruits and vegetables
Examples of products not eligible: juices, purées, pastes and powdered forms of fruits and vegetables and all forms of coconut
Milk from any animal, in liquid or powdered form
Examples of eligible products: cow, sheep and goat milk
Example of products not eligible: plant-based beverages
Whole eggs, fresh or in liquid, frozen, or dried form, or whole egg mixes
o Examples of eligible products: hard boiled eggs, quail, turkey or duck eggs, dried whole egg mix
Examples of products not eligible: liquid egg whites, plant-based egg, dried yolk mix
Nuts, seeds or their butters that contain less than 30% (<30%) of their total fat content as saturated fat
Examples of eligible products: almonds, cashews, sunflower seed butter
Examples of products not eligible: hazelnut spread, coconut
Vegetable or marine oils that contain < 30% of their total fat content as saturated fat
Examples of eligible products: olive oil, canola oil, sunflower oil
Examples of products not eligible: animal fats and oils, coconut oil, palm oil
Marine or fresh water animal products referred to in Division 21 of the FDR that contain < 30% of their total fat content as saturated fat
Examples of eligible products: salmon, trout, sardines, shellfish
Examples of products not eligible: none identified
Any combination of products above
Examples of eligible products: sardines packed in olive oil, trail mix of unsalted roasted nuts and unsweetened dried fruit, mixed cut fruit
This conditional exemption applies to these foods when they are packaged and sold as such and may also apply when these foods are included in prepackaged products that contain an assortment of foods, or prepackaged products that contain either ingredients that are intended to be combined together or foods that are intended to be consumed together. Section 7 provides more information on the application of this exemption to such products.
Reference: subsections B.01.350(6) and (10), FDR
Loss of conditional exemption: The prepackaged products lose their conditional exemption when they contain an ingredient that has saturated fat, sugars or sodium other than ingredients set out in subsections B.01.350(7) and (8) and shown in the lists below.
Ingredients that will not trigger the loss of the exemption in foods with health protection benefits
In relation to saturated fat and sodium, the following ingredients will not trigger a loss of the exemption when no saturated fat or sodium has been added to them:
whole or cut fresh, frozen, canned or dried vegetables and fruits (other than coconut)
milk from any animal, in liquid or powdered form, whether standardized or unstandardized
whole eggs, fresh or in liquid, frozen, or dried form, or whole egg mixes, whether standardized or unstandardized
nuts, seeds or their butters that contain < 30% of their total fat content as saturated fat
vegetable or marine oils that contain < 30% of their total fat content as saturated fat
marine or fresh water animal products referred to in Division 21 of the FDR that contain < 30% of their total fat content as saturated fat
Reference: subsections B.01.350(7) and (10), FDR
In relation to sugars, the following ingredients will not trigger a loss of the exemption when no sugars have been added to them:
whole or cut fresh, frozen, canned or dried vegetables and fruits (other than coconut)
milk from any animal, in liquid or powdered form, whether standardized or unstandardized
dairy products such as cheese and yogurt
nuts, seeds or their butters that contain < 30% of their total fat content as saturated fat
grains such as barley, oats and quinoa
legumes such as lentils and soybeans
Reference: subsection B.01.350(8), FDR
When the exemption is lost the total amount of the nutrient of concern in the products (from all ingredients) must be assessed to determine whether it meets or exceeds the threshold for that nutrient.
This conditional exemption is nutrient-specific. This means that a product can lose the exemption for any or all nutrients of concern.
The nutrient-specific aspect of the exemption works as follows:
Consider a can of artichoke hearts with the following list of ingredients:
Artichoke hearts are eligible for the conditional exemption under paragraph B.01.350(6)(a) whole or cut fruits or vegetables, including frozen, canned or dried fruits or vegetables.
The presence of a sodium-containing ingredient that is not provided for in subsection B.01.350(7), such as salt in this example, triggers the loss of the exemption for sodium. Therefore, the product's total sodium content needs to be assessed against the threshold. Total sodium content includes the sodium from all ingredients including any naturally occurring sodium in the artichoke hearts.
If the total sodium content meets or exceeds the threshold, the product must carry a symbol indicating that it is "high in sodium".
However, the presence of such a sodium-containing ingredient does not trigger the need to assess the total saturated fat or total sugars content against the applicable thresholds.
5.3.2.2 Foods that are important sources of calcium, a shortfall nutrient that is not readily available in other foods
The prepackaged products in this list are conditionally exempt from the symbol requirements for saturated fat and sugars:
Cheese that is made from dairy products, whether standardized or unstandardized
Yogurt, including drinkable yogurt, that is made from dairy products
Kefir
Buttermilk
This conditional exemption applies to these foods when they are packaged and sold as such and may apply when these foods are included in prepackaged products that contain an assortment of foods, or prepackaged products that contain either ingredients that are intended to be combined together or foods that are intended to be consumed together. Section 7 provides more information on the application of this exemption to such products.
To benefit from the exemption, these products must contain: ≥ 10% DV calcium per serving or reference amount, whichever is greater, for products with a reference amount of 30 g or 30 mL or less and ≥ 15% DV calcium per serving size or reference amount, whichever is greater, for products with a larger reference amount.
Reference: subsections B.01.350(9) and (12), FDR
A marketing authorization published on June 5, 2024, extends the eligibility for this exemption to products that contain ≥ 5% DV calcium per serving or reference amount, whichever is greater, regardless of the product’s reference amount.
Loss of conditional exemption: The prepackaged products lose their conditional exemption when they contain an ingredient that has saturated fat or sugars other than ingredients set out in subsection B.01.350(9), shown in the lists below.
Ingredients that will not trigger the loss of the exemption in cheese and yogurt, including drinkable yogurt, made from dairy products, kefir and buttermilk
In the case of saturated fat, the following ingredients will not trigger a loss of the exemption:
milk ingredients
modified milk ingredients
nuts or seeds that contain < 30% of their total fat content as saturated fat
vegetable or marine oils that contain < 30% of their total fat content as saturated fat
marine or fresh water animal products referred to in Division 21 of the FDR that contain < 30% of their total fat content as saturated fat
Reference: paragraph B.01.350(9)(a), FDR
In the case of sugars, the following ingredients will not trigger a loss of the exemption when no sugars have been added to them:
whole or cut fresh, frozen, canned or dried vegetables and fruits
dairy products such as milk and cream
grains such as barley, oats and quinoa
legumes such as lentils and soybeans
nuts or seeds
Reference: paragraph B.01.350(9)(b), FDR
When the exemption is lost the total amount of the nutrient of concern in the products (from all ingredients) must be assessed to determine whether it meets or exceeds the threshold for that nutrient.
As with foods that have a health protection benefit (see Section 5.3.2.1), this conditional exemption is nutrient specific. This means that a product can lose the exemption for saturated fat or sugars or both.
There is no conditional exemption from sodium for yogurt, kefir and buttermilk. Cheese that meets the calcium threshold, however, is always exempt from the requirement to assess sodium content against the threshold and will not have to display a "high in sodium" symbol.
Reference: subsection B.01.350(11), FDR
The nutrient-specific aspect of the exemption works as follows:
Consider a yogurt with the following list of ingredients:
The presence of one or more ingredients that contain sugars that is not provided for in paragraph B.01.350(9)(b), such as the milk chocolate chips and the shredded coconut preparation, triggers the loss of the exemption for sugars. Therefore, the total sugars content of the product needs to be assessed against the threshold. The presence of one or more ingredients that contain saturated fat that is not provided for in paragraph B.01.350(9)(a), such as the milk chocolate chips and shredded coconut preparation, triggers the loss of the exemption for saturated fat and therefore, the total saturated fat content of the product needs to be assessed against the threshold. Total nutrient content includes the amount in all ingredients including any naturally occurring sugars and saturated fat in the yogurt.
If the total sugars content meets or exceeds the threshold, the product must carry a symbol indicating that it is "high in sugars".
Similarly, if the total saturated fat content meets or exceeds the threshold, the product must carry a symbol indicating that it is "high in sat fat".
5.4 What exemption applies to fats and oils?
A full exemption applies to fats and oils referred to in Division 9 of the FDR, fish and other marine fats and oils, butter, ghee and margarine and other similar substitutes for butter when they are packaged and sold as such. Examples of products eligible for this exemption include bricks of butter, tubs of margarine and bottles of coconut oil. The full exemption applies to animal, fish, marine and vegetable sources of fats and oils regardless of their saturated fat content (or fatty acid profile).
A conditional exemption applies to vegetable and marine fats and oils that contain < 30% of their total fat content as saturated fat when they are packaged and sold as such and when they are ingredients in foods identified in subsection B.01.350(6).
Product-specific full exemptions and conditional exemptions may interact. For example, coconut oil is exempt from carrying a nutrition symbol when packaged and sold as such [B.01.350(5)(i), FDR]. Coconut oil has more than 30% of its total fat content as saturated fat. As a result, it does not benefit from the conditional exemption set out in B.01.350(6)(e) for vegetable oils that contain less than 30% of their total fat content as saturated fat. However, the FDR still fully exempts coconut oil, when it is sold as such, from the requirement to carry a nutrition symbol, because the provision for a full exemption takes precedence over that for the conditional exemption [B.01.350(14), FDR].
6. Presentation of the front-of-package (FOP) nutrition symbol
The Food and Drug Regulations (FDR) prescribe where and how the FOP nutrition symbol (the symbol) must be displayed on the label of a prepackaged product that meets or exceeds established thresholds for saturated fat, sugars and/or sodium.
Figure 6.1 illustrates four possible symbol formats. As shown, formats vary based on the nutrient(s) declared, number of bars, language and orientation. Schedule K.1 in the FDR contains images of the 78 unique symbol formats. However, all formats include the following mandatory design elements:
The symbol is in black and white and consists of a solid white rectangular box with a thin black line border
There is a black magnifying glass inside the box and it is left-justified
The heading "High in" appears in bold black letters inside the box at the top
There is at least one bar inside the box that identifies the product as "high in sat fat", "high in sugars" and/or "high in sodium", as applicable
The symbol is attributed to Health Canada inside the box at the bottom
The elements that make up the symbol design do not touch each other
The symbol is surrounded by a minimum buffer that is free of text and other graphic material
6.1 Where on the labels of prepackaged products does the symbol have to be displayed?
When the height of the PDP is equal to or greater than the width of the PDP, the symbol must be displayed within the upper half (50%) of the PDP as shown in Figure 6.2. The PDP of the package is shaded in the figure.
Reference: paragraph B.01.355(1)(b), FDR
When the height of the PDP is less than the width of the PDP, the symbol must be displayed within the right half (50%) of the PDP as shown in Figure 6.3. The PDP of the package is shaded in the figure.
Reference: paragraph B.01.355(1)(a), FDR
6.1.1 Cylindrical packages
On cylindrical packages, the outer edge of the buffer surrounding the symbol must be a minimum distance of 10% of the width of the principal display surface (PDS) from the left or right edge of that surface.
Reference: subsection B.01.355(3), FDR
For example, a can has a PDS with a width of 6 cm. Ten percent (10%) of the width of the PDS is equal to 0.6 cm. Therefore, the outer edge of the buffer must be at least 0.6 cm from either the left or right edge of the PDS and the symbol must be within the upper half (50%) of the PDP (Figure 6.4).
This requirement also applies to cylindrical packages on which the symbol must be displayed in the right half (50%) of the PDP. In this case, if it is not possible to display the symbol entirely in the right half of the PDP due to the requirement to be at a minimum distance from the edge of the PDS, the symbol can appear in the left half but only to the extent necessary. This means the outer edge of the buffer is as close as possible to the 10% line as shown in Figure 6.5 so that there is minimal crossing over of the symbol into the left half of the PDP.
Reference: subsection B.01.355(4), FDR
6.1.2 Irregular shapes
The upper half and right half of the PDP each refer to a proportion of the surface area of the panel. The line delineating these proportions may not correspond to the halfway point of the height measurement or width measurement of the panel, respectively. This is notably the case for products with an irregular shape PDP, as shown in Figure 6.6. The Canadian Food Inspection Agency's Industry Labelling Tool provides information on mathematical calculations for determining the area of various geometric shapes.
6.1.3 Products displayed for sale in different ways
Regulated parties are responsible to ensure that the FOP nutrition symbol appears on the PDP, which is generally on the side or surface of the container that is displayed under customary conditions of sale.
As prepackaged products may differ in the way they are displayed at the time of sale, manufacturers and importers share joint responsibility with retailers to ensure that all information is displayed on the appropriate surface at the time of sale. Mandatory information may be repeated on multiple surfaces.
6.1.4 Products with a scale label
Location of the nutrition symbol
Products with a scale label can display the symbol as a separate sticker or printed directly on the scale label. In both cases, regulated parties must first try to display the symbol in a manner that meets the requirements for symbol location as set out in B.01.355(1), FDR and described in subsection 6.1.
If it is not possible to meet the regulatory requirements for symbol location, products with a scale label may display the nutrition symbol anywhere on the scale label (Figure 6.7) or elsewhere on the PDS (Figure 6.8). This applies regardless of the establishment where they are packaged and labelled. The symbol must be visible under customary conditions of sale for the consumer. It must not cover any other mandatory information and must not be on the bottom of the container.
If placed elsewhere on the PDS, regulated parties are encouraged to display the symbol within the upper half or right half of the PDS (Figure 6.8), similar to the general location requirements described in subsection 6.1.
Symbol size
See Section 6.4 for information regarding the symbol size for products with a PDS > 250 cm2 that are sold only in the retail establishment where they are packaged and labelled by means of a sticker. This does not apply to establishments other than a retailer.
6.1.5 Ornamental and decorative containers
Ornamental container means a container that, except on the bottom, does not have any promotional or advertising material thereon, other than a trade mark or common name and that, because of any design appearing on its surface or because of its shape or texture, appears to be a decorative ornament and is sold as a decorative ornament in addition to being sold as the container of a product.
Reference: subsection B.01.001(1), FDR
Ornamental containers have the potential for an extended life, as they are reusable. Ornamental containers must be substantial enough to be sold on their own merit (without the food). They are usually made of metal (for example, cookie tins), plastic or glass (for example, candy-filled figurines).
To align with the FDR, which allow mandatory labelling information to be shown on a label that is applied to the bottom of an ornamental container, the FOP nutrition symbol can be displayed on a label that is applied to the bottom of an ornamental container. The symbol can also be displayed on a tag if one is attached to an ornamental container. No information should appear on the top of the ornamental container other than a trade mark or common name.
The container on the left in Figure 6.9 is an ornamental container. The container on the right is no longer considered an ornamental container as it has a label on the top of the container. The FOP nutrition symbol cannot be displayed on the bottom of the container on the right.
Decorative containers, although aesthetically pleasing, are usually not reusable (as opposed to ornamental containers) because they are not sturdy enough and often get torn or damaged upon opening. Fabric-covered or embossed cardboard boxes for chocolates (for example, for Valentine's Day) are normally considered decorative containers. The symbol cannot be displayed on the bottom of a decorative container.
6.2 How does the symbol have to be displayed on labels of prepackaged products?
There are requirements related to the symbol's visibility, language, orientation and graphic specifications. The nutrition symbol must be displayed in accordance with the applicable symbol set out in Schedule K.1, FDR. Regulated parties are encouraged to display the nutrition symbol in the applicable part of the PDP in such a manner that it will remain intact when the package is opened.
The nutrition symbol can be printed directly on a label or applied to it as a sticker. In the latter case, the sticker must be able to withstand any of the normal conditions that the product may be exposed to until such time the product reaches the consumer.
Section 7 provides additional information about how to display the nutrition symbols on prepackaged products containing an assortment of foods when one or more of the foods requires a nutrition symbol.
Visibility
The symbol must be clearly visible and distinguishable from all other information appearing on the PDP of the product.
Reference: section A.01.016, FDR
Language
The symbol must be presented in both official languages (English and French) unless otherwise exempt from bilingual labelling. For more information, refer to Bilingual food labelling requirements – Exemptions on the Canadian Food Inspection Agency's (CFIA) Industry Labelling tool.
Product labels can carry two separate unilingual symbols, one in French and one in English, or bilingual symbol(s). In a bilingual symbol, the order of languages may be reversed from the order shown in the applicable format (in other words, English before French or French before English).
Reference: subsections B.01.351(2) to (5), FDR
The FDR state that where there are one or more surfaces on the label of a food that are of at least the same size and prominence as the PDP, the information required by the regulations to be shown on the PDP may be shown in one official language if such information is shown in the other official language on one of those other surfaces. This means that a unilingual symbol in English can be shown on a unilingual English PDP and a unilingual symbol in French can be shown on another surface that is of at least the same size and prominence as the PDP, as illustrated in Figure 6.13
Reference: subsection B.01.012(8), FDR
Orientation
The symbol must be oriented in the same manner as most of the other information that appears on the principal display panel. However, when the panel is displayed in the vertical plane and most of the other information is not displayed parallel with the base of the package, the symbol must be oriented in such a manner that the words appearing in it are parallel with the base of the package.
Orientation also refers to either a horizontal symbol format (where its width is greater than its height) or a vertical symbol format (where its height is greater than its width).
The horizontal format is the default orientation, therefore the majority of products that need to carry the symbol will display a horizontal format.
The use of the vertical format is required when:
the product has a PDS ≤ 450 cm2, and
the horizontal format that would otherwise need to be used is wider than the PDP.
Reference: subsections B.01.351(2) and (3) and section B.01.356, FDR
Specifications
The term "specifications" refers to the symbol size (height and width), the minimum buffer surrounding the symbol, the height of letters in the symbol, the height of nutrient bars in the symbol and the diameter of the lens of the magnifying glass in the symbol. The specifications for each format are set out in the Directory of Nutrition Symbol Specifications (the Directory), which is incorporated by reference into the FDR and available on the Government of Canada website.
Section 7 provides additional information about how to display the nutrition symbols on prepackaged products containing an assortment of foods when one or more of the foods requires a nutrition symbol.
6.3 What is the minimum buffer surrounding the symbol and how is it determined?
The buffer zone is the space surrounding the symbol in which no other text or graphic material can appear. The regulations set out the minimum dimension of this zone for each symbol format. It is equal to the size of the "x" height of text in the symbol (except for the words Health Canada / Santé Canada). The "x" height is the height of the lowercase "x" in the OpenType version of the font Helvetica Neue LT STD (Figure 6.15).
6.4 What is the symbol size based on?
The size of the symbol is proportional to the PDS of the package. In other words, the height and width of the symbol decreases as the PDS decreases.
For each format, the symbol specifications shown in Figure 6.16 are set out in the Directory according to a hierarchy based on the PDS. This is a similar approach to the existing hierarchies based on the available display surface for the Nutrition Facts table formats.
The hierarchy of symbol specifications is based on the following PDS ranges:
> 600 cm2 (applies only to horizontal formats)
> 450 cm2 to ≤ 600 cm2 (applies only to horizontal formats)
> 250 cm2 to ≤ 450 cm2
> 100 cm2 to ≤ 250 cm2
> 30 cm2 to ≤ 100 cm2
≤ 30 cm2
The hierarchy of specifications (proportional to the PDS) applies in the majority of cases.
However, there is an exception for products with a PDS > 250 cm2 that are sold only in the retail establishment where they are packaged and labelled by means of a sticker. These products can carry a smaller symbol than would otherwise be required. They can carry a horizontal symbol with the specifications set out for a PDS in the range of > 100 cm2 to ≤ 250 cm2. Section 6.1.4 provides information on where the symbol can be displayed on products that have scale labels.
The symbol may be displayed with larger dimensions than those set out in Column 3 of the applicable table in the Directory if it is scaled in a proportional manner vertically and horizontally.
Reference: Directory of Nutrition Symbol Specifications and section B.01.352, FDR
6.5 How many bars have to appear in the symbol?
The number of bars that have to appear in the symbol depends on the PDS and the number of nutrients that must be declared.
PDS > 30 cm2
Three bars must always appear in the symbol on packages with a PDS > 30 cm2. This includes the bars required to identify the product as "high in sat fat", "high in sugars" and/or "high in sodium" (nutrient bars), as applicable, and blank bars. This ensures the nutrients are always in the same order.
The following are examples of formats for use on packages with a PDS > 30 cm2. Each has three bars in total; however, the number of nutrient bars and blank bars varies.
PDS ≤ 30 cm2
The only bars that must appear in the symbol on packages with a PDS of ≤ 30 cm2 are the bars required to identify the product as "high in sat fat", "high in sugars" and/or "high in sodium", as applicable. Blank bars are not required to be shown. Therefore, some small packages may display symbols with fewer than three bars.
The following are examples of formats for use on packages with a PDS ≤ 30 cm2.
6.6 In what order do the nutrient bars have to appear in the symbol?
The order of the nutrient bars in the symbol is always:
Sat fat
Sugars
Sodium
In symbol formats with three bars, the top bar is always and only for saturated fat, the middle bar is always and only for sugars and the bottom bar is always and only for sodium. The order doesn't change because of blank bars.
6.7 How are the different symbol formats identified in the regulations?
Each symbol format is identified by the same unique number and letter combination in the table to B.01.352, Schedule K.1 and the Directory. Numbers distinguish formats based on nutrient combination and letters indicate language and symbol orientation. The diagram in Figure 6.19 further describes this naming convention.
6.8 How can I obtain high resolution graphic files of all variations of the symbol?
A Compendium of Nutrition Symbol Formats (the Compendium) is available in PDF as a reference document for label designers and the food and packaging industry to comply with the format specifications set out in the FDR and in the Directory. Ready-to-use high resolution graphic files of all variations of the symbol are available in .EPS format. To obtain a copy of the Compendium and the graphic files, please send an e-mail to smiu-ugdi@hc-sc.gc.ca with the subject line "HPFB BNS Compendium of Nutrition Symbol Formats".
In addition to the number and letter combination used in the naming convention in the regulations, the Compendium includes a number to distinguish the figures based on the PDS (Figure 6.20). For example, consider a product with a PDS > 600 cm2, which requires symbol format 6(BH) as per the naming convention used in the regulations. In the Compendium, this is the symbol format equivalent to Figure 1.6(BH). Appendix A in the Compendium shows how these different conventions align.
7. Front-of-package (FOP) nutrition labelling of prepackaged products that contain assortments of foods, and prepackaged products that contain either ingredients that are intended to be combined together or foods that are intended to be consumed together
This section provides information on the following three topics as they relate to prepackaged products that contain an assortment of foods and prepackaged products that contain either ingredients that are intended to be combined or foods that are intended to be consumed together:
assessment of saturated fat, sugars and sodium content against the % daily value (DV) thresholds
conditional exemptions set out in subsections B.01.350(6) to (12)
symbol presentation where one or more of the foods in these types of products require a nutrition symbol.
7.1 How does FOP nutrition labelling apply to prepackaged products that contain an assortment of foods?
Assessment of saturated fat, sugars and sodium content against thresholds
For prepackaged products that contain an assortment of foods, the nutrient content assessment may align with the format of the Nutrition Facts table (NFt): standard or aggregate. This flexibility means that:
For assortments with an aggregate NFt, such as a multi-pack of granola bars, the nutrient content of each food in the assortment is assessed against the threshold individually.
For assortments with a standard NFt with composite values, such as a box of assorted chocolates, the nutrient content of the composite can be assessed against the threshold.
For assortments of similar types of foods, such as a multi-pack of frozen popsicles, where a serving consists of only one of the foods and where information for serving size, energy and core nutrients is the same for all individual items and must be set out in a standard NFt, the nutrient content of any one item is assessed against the threshold.
Section 4 provides information on the % DV thresholds and the approach for determining whether the amount of saturated fat, sugars and/or sodium in a prepackaged product meets or exceeds them.
Conditional exemptions
The conditional exemptions set out in subsections B.01.350(6) to (12), FDR, can be applied to prepackaged products that contain an assortment of foods.
When assortments carry an aggregate NFt, the nutrient content of each food in the assortment is assessed against the threshold individually. As a result, each food maintains the exemption that would apply to it when packaged and sold as such.
When assortments contain only foods set out in subsection B.01.350(6) or in subsection B.01.350(9) and are labelled with composite values in a standard NFt, the exemption applies to the product as a whole.
Section 5.3.2 provides information on the exemptions set out in subsections B.01.350(6) to (12).
Symbol presentation where one or more of the foods require a nutrition symbol
If a prepackaged product contains an assortment of foods and one or more of the foods require a nutrition symbol, the nutrition symbols must be displayed in a manner that clearly indicates the applicable nutrients that are contained in each food.
Reference: subsection B.01.353(1), FDR
Examples of acceptable symbol presentation for assortments where one or more foods requires a symbol
It is acceptable to place the name of the food, variety or flavour in the assortment that requires a symbol immediately adjacent to the buffer zone of the applicable symbol as shown in Figure 7.1. The use of an image that clearly identifies the food, variety or flavour is also acceptable (Figure 7.2). Note that text or other graphic material cannot appear in the buffer zone (B.01.355(2)(b), FDR).
When more than one food, variety or flavour in an assortment require the same nutrition symbol, regulated parties do not need to duplicate the symbol on the PDP. The symbol can be displayed only once if the food, variety or flavour it applies to is clearly indicated (Figure 7.3).
Furthermore, when all foods, varieties or flavours in an assortment require the same symbol, regulated parties must clearly indicate that the symbol applies to all items in the assortment.
Consider a multi-pack of frozen popsicles in three flavours. All three flavours have the same nutrition information and the product must carry the standard format NFt. The nutrient content of one flavour is assessed. It is determined that the sugars content exceeds the % DV threshold. The "high in sugars" symbol must be displayed in a manner that clearly indicates it applies to the three flavours (Figure 7.4). The symbol does not need to be shown three times.
Any text used to meet the requirement in subsection B.01.353(1) must meet bilingual requirements, if applicable. The text must be clearly and prominently displayed on the label and readily discernible to the purchaser or consumer under the customary conditions of purchase.
References: section A.01.016 and subsection B.01.012(2), FDR
When more than one food in an assortment requires a symbol, the buffer zones can overlap in the space between the symbols as shown in Figure 7.5.
Examples of unacceptable presentation for assortments where one or more foods require a nutrition symbol
Using a legend to indicate which nutrient in a nutrition symbol applies to which food, variety or flavour (Figure 7.6)
Associating one food, variety or flavour to more than one nutrition symbol (Figure 7.7)
Displaying only the nutrition symbol for the food, variety or flavour with the most "high in" nutrients and referring the consumer to the NFt for information on the other foods (Figure 7.8)
Table 7.1. Summary of requirements and flexibilities for prepackaged products that contain an assortment of foods
Description of the prepackaged product
Examples
NFt format
Nutrient content assessment (saturated fat, sugars, sodium) and application of conditional exemptions set out in B.01.350(6) to (12)
Nutrition symbol presentation where one or more foods require a symbol
Assortment of foods of the same type where:
a typical serving consists of only one of the foods and
the nutrition information for each food is different
Multi-pack of instant oatmeal
Multi-pack of granola bars
These products must use the aggregate NFt with information declared for each food in the assortment (B.01.406(3)(a), FDR)
Each food in the assortment is assessed against the threshold
Conditional exemptions apply to eligible foods individually
More than one symbol could be required
Symbols must be displayed in a manner that clearly indicates to which food they apply (B.01.353(1), FDR)
Assortment of foods of the same type where:
a typical serving consists of only one of the foods and
the nutrition information for each food is the same
Multi-pack of popsicles
Multi-pack of yogurt
These products must use the standard NFt with information declared for one of the foods (B.01.406(3)(b), FDR)
Any food in the assortment is assessed against the threshold as the nutrition information is the same for all foods in the package
Conditional exemptions apply to eligible foods
One symbol could be required
Symbol must be displayed in a manner that clearly indicates it applies to all foods in the assortment (B.01.353(1), FDR)
Assortment of foods of the same type where:
a typical serving consists of more than one of the foods
Tray of mixed nuts
Box of assorted chocolate
Tin of assorted cookies
These products can use the aggregate NFt with information declared for each food in the assortment or the standard NFt with composite values (B.01.406(4), FDR)
When the product carries the aggregate NFt:
Each food in the assortment is assessed against the threshold
Conditional exemptions apply to eligible foods individually
More than one symbol could be required
Symbols must be displayed in a manner that clearly indicates to which food they apply (B.01.353(1), FDR)
When the product carries the standard NFt:
The composite can be assessed against the threshold
Conditional exemptions apply to product as a whole
One symbol could be required
No requirement to indicate that the symbol applies to the composite or each food
Assortment of foods of different types intended to be consumed together
Charcuterie tray
Assorted appetizers and sauces
These products can use the aggregate NFt with information declared for each food (B.01.406(2), FDR)
Each food in the assortment is assessed against the threshold
Conditional exemptions apply to eligible foods individually
More than one symbol could be required
Symbols must be displayed in a manner that clearly indicates to which food they apply (B.01.353(1), FDR)
Consider an assortment that contains plain roasted almonds, cheddar cheese, ham and cookies. The product carries an aggregate NFt with information declared for each food in the assortment. The almonds are eligible for the conditional exemption set out in paragraph B.01.350(6)(d) and the cheddar cheese is eligible for the conditional exemption set out in subsections B.0.350(9) and (11). Assuming the almonds are roasted with an oil with a healthy fat profile and the cheddar cheese meets the calcium threshold set out in subsection B.01.350(12), regulated parties are not required to assess the nutrient content of these two foods against the % DV thresholds. (Section 5.3.2 provides more information about these conditional exemptions.) It is determined that the sodium content of the ham exceeds the threshold as does the sugars content of the cookies. It must be clearly indicated that the "high in sodium" symbol applies to the ham and the "high in sugars" symbol applies to the cookies.
Consider an assortment that contains two varieties of plain nuts and two varieties of seasoned nuts. The product carries the standard format NFt with information declared as a single composite value. The product as a whole is eligible for the conditional exemption set out in paragraph B.01.350(6)(d). The product loses the conditional exemption for sodium because of the salt used in the seasoned nuts. (Section 5.3.2 provides more information about the conditional exemption.) The total sodium content of the product as a whole is assessed against the % DV threshold; total sodium content includes the sodium in the seasoned nuts and the naturally occurring sodium in the plain nuts. It is determined that the sodium content meets the threshold. The product maintains the conditional exemption from the requirement to assess saturated fat and sugars content. The label must display the "high in sodium" symbol. There is no requirement to indicate that the symbol applies to the product as a whole.
7.2 How does FOP nutrition labelling apply to prepackaged products that contain either ingredients intended to be combined together or foods intended to be consumed together?
Assessment of saturated fat, sugars and sodium content against thresholds
For prepackaged products that contain either ingredients intended to be combined together or foods intended to be consumed together, the nutrient content assessment may align with the format of the Nutrition Facts table (NFt): standard or aggregate. This flexibility means that:
When these products carry a standard or aggregate NFt, such as hors d'oeuvres with sauce, the nutrient content of the product as a whole (ingredients or foods combined) is assessed against the threshold. A reference amount for the product as a whole is required.
Alternatively, when these products carry an aggregate NFt, the nutrient content of each ingredient or food can be assessed against the threshold individually.
Section 4 provides information on the % DV thresholds and the approach for determining whether the amount of saturated fat, sugars and/or sodium in a prepackaged product meets or exceeds them.
Conditional exemptions
The conditional exemptions set out in subsections B.01.350(6) to (12), FDR, can be applied to prepackaged products that contain either ingredients intended to be combined together or foods intended to be consumed together.
When these products carry an aggregate NFt and the nutrient content of each food or ingredient is assessed against the threshold individually, the exemptions apply to each food or ingredient. As a result, each food can maintain the exemption that would apply to it when packaged and sold as such.
When these products carry a standard or aggregate NFt and the nutrient content of the product as a whole is assessed against the threshold, the exemptions apply to the product as a whole. As a result, the product can maintain the exemption set out in subsection B.01.350(6) if the product contains only foods in that subsection.
Section 5.3.2 provides information on the exemptions set out in subsections B.01.350(6) to (12).
Symbol presentation where one or more of the foods require a nutrition symbol
Subject to subsection B.01.353(2) of the FDR, if a prepackaged product contains either ingredients that are intended to be combined together or foods that are intended to be consumed together, the nutrition symbol must display the nutrients that are contained in the product as a whole. No further indication near the FOP symbol would be required.
However, if a prepackaged product contains either ingredients that are intended to be combined together or foods that are intended to be consumed together, carries an aggregate NFt and one or more of the ingredients or foods require a nutrition symbol, regulated parties are encouraged to display the symbols in a manner that clearly indicates the applicable nutrients that are contained in each ingredient or food as described in Section 7.1.
Table 7.2. Summary of requirements and flexibilities for prepackaged products that contain either ingredients that are intended to be combined together or foods that are intended to be consumed together
Description of the prepackaged product
Examples
NFt format
Nutrient content assessment (saturated fat, sugars, sodium) and application of conditional exemptions set out in B.01.350(6) to (12)
Nutrition symbol presentation where one or more foods or ingredients require a symbol
Prepackaged products that contain either ingredients that are intended to be combined together or foods that are intended to be consumed together
Sushi rolls and sauce
Chicken wings and sauce
Taco kit
Salad kit
Cheese and cracker snack pack
Yogurt with granola topping
These products can use the standard NFt with values for the product as a whole or the aggregate NFt with information declared for each ingredient or food (B.01.406(2), FDR)
When the product carries the standard or aggregate NFt:
The nutrient content of the product as a whole is assessed against the threshold. A reference amount for the product as a whole is required
Conditional exemption set out in subsection B.01.350(6) applies to product as a whole if it contains only foods set out in paragraphs (a) to (g)
One symbol could be required
The symbol must display the nutrients that are contained in the product as a whole (B.01.353(2), FDR). No requirement to indicate that the symbol applies to the entire product
When the product carries the aggregate NFt:
Each ingredient or food can also be assessed against the threshold
Conditional exemptions apply to eligible ingredients or foods individually
More than one symbol could be required
Regulated parties are encouraged to display the symbols in a manner that clearly indicates to which food they apply
Consider a prepackaged product that contains chicken wings and 2 dipping sauces. The foods are intended to be consumed together and the product carries an aggregate NFt with information declared for each food. Each food is assessed against the % DV threshold to determine whether one or more of the foods require a symbol. If one or more foods require a symbol, regulated parties are encouraged to display the symbols in a manner that clearly indicates to which food they apply.
Consider a salad kit that contains mixed greens, apples, dried unsweetened cranberries, plain almonds, bacon and creamy dressing. The ingredients are intended to be combined together and the product carries a standard NFt with information declared for the product as a whole. The conditional exemption set out in subsection B.01.350(6) does not apply because the product contains foods other than those referred to in paragraphs (a) to (f). The saturated fat, sugars and sodium content of the product as a whole is assessed against the % DV threshold to determine whether the product requires a nutrition symbol.
8. Nutrient and health-related claims and the front-of-package (FOP) nutrition symbol
For the purposes of FOP nutrition labelling, in subsection B.01.357(3), the regulations define "health-related representation" as:
Health-related representation means
Examples
(a) a declaration referred to in subsection B.01.301(1) or (2)
Quantitative declarations outside of the Nutrition Facts table "360 mg of calcium per bar (40 g)"
(b) a statement or claim referred to in subsection B.01.311(2) or (3)
Nutrient function claims "Protein helps build strong muscles"
(c) a representation referred to in any of sections B.01.503 to B.01.513
Nutrient content claims "Reduced in sugar"
(d) a statement or claim referred to in subsection B.01.601(1)
Health claims "A healthy diet rich in a variety of vegetables and fruit may help reduce the risk of heart disease."
(e) any other health-related statement, logo, symbol, seal of approval or mark
The use of a name, logo, symbol, seal of approval or other certification mark of a third party-organization Using a check mark to draw attention to good or healthy choices.
Nutrition and health-related statements and claims may be made on the label or in advertisements for foods on a voluntary basis. However, when they are made, they must comply with subsection 5(1) of the Food and Drugs Act, the food provisions of the FDR, and subsection 6(1) of the Safe Food for Canadians Act and should follow any applicable guidance.
8.1 Are health-related representations permitted on the principal display panel (PDP) when a food also carries the FOP nutrition symbol (the symbol)?
Yes. Most health-related representations are permitted on the PDP when it displays the symbol. This includes representations not related to saturated fat, sugars or sodium (for example, protein, fibre or energy) and representations that are related to these nutrients of concern as long as there is no "high in" symbol for that nutrient on the PDP. For example, a "low sodium" claim is permitted on the PDP when the product carries a "high in sat fat" symbol. Statements or claims described in sections D.01.004 to D.01.007 and D.02.002 to D.02.005 are also permitted on the PDP when it carries a symbol. However, the "unsweetened" claim is prohibited on the PDP when it carries a symbol for "high in sugars" and the representation that a food is for use in a sodium-restricted diet is prohibited when the PDP carries a symbol for "high in sodium".
Furthermore, all nutrient content claims related to saturated fat, sugars or sodium, as set out in the Table of Permitted Nutrient Content Statements and Claims (the Table) incorporated by reference into the FDR, are prohibited on the PDP when it carries a symbol to identify the food as "high in" that particular nutrient, except for "reduced in" claims.
For instance, the claims related to saturated fat set out in item 18, 19 and 21 of the Table are prohibited on the PDP when it carries a symbol for "high in sat fat". The "reduced in saturated fatty acids" claim (item 20) is the only claim about saturated fat in the Table that is permitted on the PDP when it carries a symbol for "high in sat fat". The nutrient content claims "lean" and "extra lean" set out in item 46 and 47 of the Table are considered related to the total fat content of a meat or poultry that has not been ground, a marine or fresh water animal or a product of any of these. These claims are not considered related to saturated fat and are not prohibited on the PDP when it carries a symbol for "high in sat fat".
The same applies to claims about sugars and sodium set out in column 4 of the Table:
The claims related to sugars set out in item 37, 37.1, 39 and 40 of the Table are prohibited on the PDP when it carries a symbol for "high in sugars". The "reduced in sugar" claim (item 38) is the only claim about sugars in the Table that is permitted on the PDP when it carries a symbol for "high in sugars".
The claims related to sodium set out in item 31, 32, 34 and 35 of the Table are prohibited on the PDP when it carries a symbol for "high in sodium". The "reduced in sodium or salt" claim (item 33) is the only claim about sodium in the Table that is permitted on the PDP when it carries a symbol for "high in sodium".
Using a representation such as a word, phrase, illustration, sign, mark, symbol or design that could be mistaken for the symbol is also prohibited regardless of whether the food carries the symbol. Note that a representation does not include a supplemented food caution identifier.
8.2 Do restrictions apply to the size of health-related representations displayed on the PDP when a food also carries the symbol?
Yes. There are limits on the size (in other words, the height of letters) of any health-related representation defined in subsection B.01.357(3) and any statement or claim described in sections D.01.004 to D.01.007 and D.02.002 to D.02.005 displayed on a PDP that carries the symbol. The maximum permitted height of the letters in the claims, statements or representations depends on whether the nutrient they feature is declared in the symbol.
However, these size limits do not apply to the brand name or product name that appear on the PDP, such as those that include the name of a nutrient or nutritive substance, for example "fibre" or "probiotics".
When the nutrient featured in a health-related representation displayed on the PDP is also declared in the symbol:
the height of the upper case letters in the claim, statement or representation must not exceed the prescribed height of the upper case letters (excluding any accents) in the applicable symbol format, other than in the words "Health Canada" and "Santé Canada"; and
the height of the tallest ascender of the lower case letters in the claim, statement or representation must not exceed the prescribed height of the tallest ascender of the lower case letters in the applicable symbol, other than in the words "Health Canada" and "Santé Canada".
When the nutrient featured in a health-related representation or a statement or claim referred to in any of sections D.01.004 to D.01.007 and D.02.002 to D.02.005 displayed on the PDP is not declared in the symbol:
the height of the upper case letters in the claim, statement or representation must not exceed two times the prescribed height of the upper case letters (excluding any accents) in the applicable symbol format, other than in the words "Health Canada" and "Santé Canada"; and
the height of the tallest ascender of the lower case letters in the claim, statement or representation must not exceed two times the prescribed height of the tallest ascender of the lower case letters in the applicable symbol format, other than in the words "Health Canada" and "Santé Canada".
The Directory of Nutrition Symbol Specifications (the Directory) sets out the height of upper case letters and tallest ascender of lower case letters that must be used in each symbol format. The information is in column 5 of each table in the Directory. See the Presentation section for more information on how to identify which symbol format must appear on the PDP.
Reference: section B.01.357 and D.01.001.2, FDR
8.3 Do restrictions apply to health-related representations displayed elsewhere than with the symbol on the PDP ?
No. Restrictions on use and size only apply to health-related representations when they are displayed with the FOP nutrition symbol on the PDP. No restrictions apply to health-related representations that appear elsewhere than on the PDP with the symbol, for example, on the back of the package. Note that these representations remain subject to existing legibility requirements.
9. Definitions
The Food and Drug Regulations (FDR) should be referred to for definitions. The definitions in this section are provided for ease of reference only.
Daily value: As defined in subsection B.01.001(1) of the FDR, means, in respect of a nutrient, the quantity applicable to the nutrient according to subsection B.01.001.1(2).
Main dish: As defined in subsection B.01.001(1) of the FDR, means a combination dish, as set out in the Table of Reference Amounts, that does not require the addition of ingredients, other than water, for its preparation and that contains food from at least two of the following categories:
dairy products and their alternatives, except butter, cream, sour cream, ice cream, ice milk, sherbet and alternatives for those foods;
meat products, poultry products, marine and fresh water animal products referred to in Division 21, and their alternatives such as eggs, tofu, legumes, nuts, seeds, nut or seed butters and spreads made from legumes;
fruits and vegetables except pickles, relishes, olives and garnishes; and
breads, breakfast cereals, rice and other grains, and alimentary pastes.
Milk ingredients: As defined in item 7 of Table 2 in the Common Names for Ingredients and Components Document, which is incorporated by reference into the FDR, means any of the following in liquid, concentrated, dry, frozen or reconstituted form, namely, butter, buttermilk, butter oil, milk fat, cream, milk, partly skimmed milk, skim milk and any other component of milk the chemical composition of which has not been altered and that exists in the food in the same chemical state in which it is found in milk.
Modified milk ingredients: As defined in item 7.1 of Table 2 in the Common Names for Ingredients and Components Document, which is incorporated by reference into the FDR, means any of the following in liquid, concentrated, dry, frozen or reconstituted form, namely, calcium-reduced skim milk (obtained by the ion-exchange process), casein, caseinates, cultured milk products, milk serum proteins, ultrafiltered milk, whey, whey butter, whey cream and any other component of milk the chemical state of which has been altered from that in which it is found in milk. As defined in item 7.2 of the Common Names for Ingredients and Components Document, which is incorporated by reference into the FDR, it also means one or more ingredients or components set out in item 7 combined with any one or more ingredients or components set out in item 7.1.
Nutrition symbol: As defined in subsection B.01.001(1) of the FDR, means a symbol set out in Schedule K.1 that is carried on the principal display panel (PDP) of a prepackaged product.
Principal display panel (PDP): As defined subsection B.01.001(1) of the FDR, means, despite the meaning assigned to that term in section A.01.010:
in the case of a label that is applied to a consumer prepackaged food within the meaning of section 1 of the Safe Food for Canadians Regulations, the principal display panel as described in paragraphs (a) to (c) of the definition of that term in that section;
in the case of a label that is applied to a prepackaged product other than a consumer prepackaged food subject to the Safe Food for Canadians Regulations, the part of the label that is applied to all or part of any side or surface of the container that is displayed or visible under normal or customary conditions of sale or use and, if the container does not have such a side or surface, the part of the label that is applied to any part of the container except on the bottom; or
in the case of a label that is applied to a food that is not a prepackaged product, the part of the label that is applied to all or part of the side or surface of the food that is displayed or visible under normal or customary conditions of sale or use.
Principal display surface (PDS): As defined in subsection B.01.001(1) of the FDR and in respect of a prepackaged product, means:
if the package has a surface that is displayed or visible under customary conditions of sale or use, the total area of that surface, excluding any surface that is the top of the package;
For example, the front panel of this cereal box, is usually visible when the product is displayed for sale. Therefore, the total area of that panel is considered the PDS, which is the area shown here with crosshatching. The grey shaded area is considered the PDP.
if the package has a lid that is the part of the package that is displayed or visible under customary conditions of sale or use, the total area of the top surface of the lid;
For example, the lid of this hummus container is usually visible when displayed for sale. Therefore, the total area of the lid is considered the PDS, which is the area shown here with crosshatching. The grey shaded area is considered the PDP.
if the package does not have a particular surface that is displayed or visible under customary conditions of sale or use, 40% of the total surface area of the package, excluding any surface area that is its top and bottom, if it is possible for that proportion of the total surface area to be displayed or visible under customary conditions of sale or use;
For example, cylindrical shaped packages, such as this soup can, don't have a particular surface that is usually visible when displayed for sale. Therefore, 40% of the package's total surface area, excluding the top and bottom is considered the PDS. It is the area shown here with crosshatching. The grey shaded area is considered the PDP.
This definition also applies to cylindrical containers that do not have a constant diameter such as this jar of toffee peanuts, in which the PDS is shown here with crosshatching. The grey shaded area is considered the PDP.
if the package is a bag with surfaces of equal dimensions, the total area of one of the surfaces;
For example, the surfaces of this bag of popcorn are the same size. Therefore, the total area of one surface is considered the PDS. It is the area shown here with crosshatching. The grey shaded area is considered the PDP.
if the package is a bag with surfaces of different dimensions, the total area of one of the largest surfaces;
For example, the surfaces of this bag of mini brownies are different sizes. Therefore, the total area of the largest surface is considered the PDS. It is the area shown here with crosshatching. The grey shaded area is considered the PDP.
despite paragraphs (a) to (e), if the package does not have a surface that is displayed or visible under customary conditions of sale or use to which a label can be applied, the total area of one side of a tag that is attached to the package;
For example, given that a mesh bag such as this one containing individually wrapped chocolates doesn't have a surface on which a label can be applied, the total area of one side of the tag attached to the bag is considered the PDS. It is the area shown here with crosshatching. The grey shaded area is considered the PDP.
despite paragraphs (a) to (e), if the package contains wine that is exposed for sale, any part of the surface of the package, excluding its top and bottom, that can be seen without having to turn the package; and
if the package is a wrapper or confining band that is so narrow in relation to the size of the food it contains that it cannot reasonably be considered to have any surface that is displayed or visible under customary conditions of sale or use, the total area of one side of a tag that is attached to the package.
Reference amount: As defined in subsection B.01.001(1) of the FDR, means, in respect of a food set out in column 1 of the Table of Reference Amounts, the amount of that food set out in column 2.
Serving of stated size: The serving size is a specific amount of food upon which the nutrient information presented in the nutrition facts table is based. The serving size is a quantity of food that can be reasonably consumed at a single eating occasion.
Sweetening agent: As defined in subsection B.01.001(1) of the FDR, includes any food for which a standard is provided in Division 18, but does not include those food additives listed in the tables to Division 16.
Appendix 1: Steps for determining whether the amount of saturated fat, sugars and/or sodium in a prepackaged product meets or exceeds the FOP nutrition symbol thresholds
These instructions describe the steps to determine whether the amount of saturated fat, sugars and/or sodium in a food meets or exceeds the applicable thresholds and triggers the need to display the FOP nutrition symbol (the symbol) on the label. Although most prepackaged products are subject to the FOP nutrition symbol labelling requirements, some foods are exempted from carrying the symbol, and in some cases, the symbol is prohibited on the label of certain foods. See the Exemptions and Prohibitions sections for more information.
Examples A to F illustrate the following scenarios:
Example A : the serving of stated size (serving size) is greater than the reference amount (food contains trans fat)
Example B : the serving size is greater than the reference amount (food does not contain trans fat)
Example C : the reference amount is greater than the serving size
Example D : the food requires preparation and has a reference amount for its unprepared form
Example E : the serving size is greater than the reference amount and the product is intended solely for children one year or older but less than four years of age
Example F : the serving size and reference amount are equal and the food has a reference amount ≤ (less than or equal to) 30 g or 30 mL
Example A –the serving of stated size (serving size) is greater than the reference amount (food contains trans fat)
This example illustrates a scenario in which the serving of stated size (serving size) declared in the Nutrition Facts table (NFt) is larger than the reference amount set out for the food in the Table of Reference Amounts.
Consider a frozen, uncooked lamb burger. The serving size declared in the NFt is 1 burger (142 g). These instructions describe the steps to follow to determine whether the amount of saturated fat, sugars and/or sodium meets or exceeds the applicable threshold and therefore, triggers the need to carry the front-of-package (FOP) nutrition symbol (the symbol) on the label.
Identify for whom the product is intended.
Determine which of the following 2 categories applies to the food:
A food intended solely for children one year of age or older, but less than four years of age (children one to four years only).
A food intended for children one year of age or older, but less than four years of age or for children four years of age or older and adults (children and/or adults).
In this example, the product is intended for children and/or adults. Therefore, the thresholds in columns 2 to 4 of the table to section B.01.350 (Thresholds Requiring a Nutrition Symbol) apply.
Identify the quantity of food that must be used to assess the amount of saturated fat, sugars and/or sodium against the symbol threshold.
Consult the Table of Reference Amounts to identify the amount applicable to the product.
The reference amount for raw patties is 100 g; it is set out in Item L.7, Column 2, of the Table of Reference Amounts.
Compare the product's reference amount and the serving size declared in the NFt. The larger quantity must be used as the base quantity for the nutrient content assessment.
In this example, the serving size (142 g) is greater than the reference amount. Therefore, the serving size is the base quantity that must be used for the assessment.
Identify the applicable % Daily Value (% DV) threshold.
Determine in which of the following classes the product belongs:
Prepackaged products with a reference amount ≤ (less than or equal to) 30 g or 30 mL: threshold of ≥ (greater than or equal to) 10% DV
Prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults): threshold of ≥ 30% DV
Prepackaged products with a reference amount > 30 g or 30 mL other than main dishes: threshold of ≥ 15% DV
In this example, the applicable threshold is ≥ 15% DV given that raw patties have a reference amount > (greater than) 30 g or 30 mL and are not a main dish.
Determine whether the amount of saturated fat, sugars and/or sodium in the base quantity meets or exceeds the threshold.
When the serving size is the base quantity for the nutrient content assessment the % DV for sugars and sodium declared in the NFt can be compared to the % DV thresholds identified in Step 3. It is important to note that the NFt presents the % DV for saturated fat andtransfat content combined and that for FOP labelling purposes, only saturated fat content must be considered when calculating the % DV to determine whether a "high in sat fat" symbol is required. If a food contains trans fat, the % DV for saturated and trans fat content declared in the NFt should not be compared to the % DV threshold for the symbol. If a food contains no trans fat, the % DV for saturated and trans fat content declared in the NFt can be compared to the threshold.
If the % DV for one or more of the nutrients is equal to or greater than the % DV threshold, a symbol for the nutrient or nutrients is required.
In this example, the product contains trans fat. For FOP labelling purposes, the % DV must only reflect saturated fat content. The % DV for saturated fat and trans fat declared in the NFt should not be compared to the % DV threshold for saturated fat.
The % DV should be calculated as follows: (saturated fat content declared in the NFt / DV for the sum of saturated fatty acids and trans fatty acids) x 100 = (10 g / 20 g) x 100 = 50%
The % DV for sugars (0%) and sodium (17%) declared in the NFt were compared to the 15% DV threshold.
In this example, the % DV calculated for saturated fat and the % DV for sodium declared in the NFt are equal to or greater than the 15% DV threshold. Therefore, the label must carry a symbol for "high in sat fat and sodium ".
See the Presentation section for more information on the symbol location and presentation requirements.
Example B – the serving size is greater than the reference amount (food does not contain trans fat)
This example illustrates a scenario in which the serving of stated size (serving size) declared in the Nutrition Facts table (NFt) is larger than the reference amount set out for the food in the Table of Reference Amounts
Consider frozen, uncooked plant-based burgers. The serving size declared in the NFt is 1 burger (113 g). These instructions describe the steps to follow to determine whether the amount of saturated fat, sugars and/or sodium meets or exceeds the applicable threshold and therefore, triggers the need to carry the front-of-package (FOP) nutrition symbol (the symbol) on the label.
Identify for whom the product is intended.
Determine which of the following 2 categories applies to the food:
A food intended solely for children one year of age or older, but less than four years of age (children one to four years only).
A food intended for children one year of age or older, but less than four years of age or for children four years of age or older and adults (children and/or adults).
In this example, the product is intended for children and/or adults. Therefore, the thresholds in columns 2 to 4 of the table to section B.01.350 (Thresholds Requiring a Nutrition Symbol) apply.
Identify the quantity of food that must be used to assess the amount of saturated fat, sugars and/or sodium against the symbol threshold.
Consult the Table of Reference Amounts to identify the amount applicable to the product.
The reference amount for raw burger patties is 100 g; it is set out in Item L.7, Column 2, of the Table of Reference Amounts.
Compare the product's reference amount and the serving size declared in the NFt. The larger quantity must be used as the base quantity for the nutrient content assessment.
In this example, the serving size (113 g) is greater than the reference amount. Therefore, the serving size is the base quantity that must be used for the assessment.
Identify the applicable % Daily Value (% DV) threshold.
Determine in which of the following classes the product belongs:
Prepackaged products with a reference amount ≤ (less than or equal to) 30 g or 30 mL: threshold of ≥ (greater than or equal to) 10% DV
Prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults): threshold of ≥ 30% DV
Prepackaged products with a reference amount > 30 g or 30 mL other than main dishes: threshold of ≥ 15% DV
In this example, the applicable threshold is ≥ 15% DV given that burger patties have a reference amount > 30 g and are not a main dish.
Determine whether the amount of saturated fat, sugars and/or sodium in the base quantity meets or exceeds the threshold
When the serving size is the base quantity for the nutrient content assessment the % DV for sugars and sodium declared in the NFt can be compared to the % DV thresholds for the symbol identified in Step 3. It is important to note that the NFt presents the % DV for saturated fat and trans fat content combined and that for FOP labelling purposes, only saturated fat content must be considered when calculating the % DV to determine whether a "high in sat fat" symbol is required. If a food contains trans fat, the % DV for saturated and trans fat content declared in the NFt should not be compared to the % DV threshold for the symbol. If a food contains no trans fat, the % DV for saturated and trans fat content declared in the NFt can be compared to the threshold.
If the % DV for one or more of the nutrients is equal to or greater than the % DV threshold, a symbol for the nutrient or nutrients is required.
In this example, the % DV declared for saturated fat and trans fat in the NFt (35%) can be compared to the % DV thresholds because the food contains no trans fat.
The % DV for sugars (0%) and sodium (17%) declared in the NFt were also compared to the 15% DV threshold.
In this example, the % DV for saturated fat and sodium meet or exceed the threshold. The label must carry a symbol for "high in sat fat and sodium".
See Presentation section for more information on the symbol location and presentation requirements.
Example C – the reference amount is greater than the serving size
This example illustrates a scenario in which the reference amount set out for the food in the Table of Reference Amounts is larger than the serving of stated size (serving size) declared in the Nutrition Facts table (NFt).
Consider a lasagna sold in a 227 g tray. The serving size declared in the NFt is 1 package (227 g). These instructions describe the steps to follow to determine whether the amount of saturated fat, sugars and/or sodium meets or exceeds the applicable threshold and therefore, triggers the need to display the front-of-package (FOP) nutrition symbol (the symbol) on the label.
Identify for whom the product is intended.
Determine which of the following 2 categories applies to the food:
A food intended solely for children one year of age or older, but less than four years of age (children one to four years only).
A food intended for children one year of age or older, but less than four years of age or for children four years of age or older and adults (children and/or adults).
In this example, the product is intended for children and/or adults. Therefore, the thresholds in columns 2 to 4 of the table to section B.01.350 (Thresholds Requiring a Nutrition Symbol) apply.
Identify the quantity of food that must be used to assess the amount of saturated fat, sugars and/or sodium against the symbol threshold.
Consult the Table of Reference Amounts to identify the amount applicable to the product.
The reference amount for lasagna is 300 g; it is set out in Item N.1, Column 2, of the Table of Reference Amounts.
Compare the product's reference amount and the serving size declared in the NFt. The larger quantity must be used as the base quantity for the nutrient content assessment.
In this example, the reference amount is greater than the serving size (227 g). Therefore, the reference amount is the base quantity that must be used for the assessment.
Identify the applicable % Daily Value (% DV) threshold.
Determine in which of the following classes the product belongs:
Prepackaged products with a reference amount ≤ 30 g or 30 mL: threshold of ≥ 10% DV
Prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults): threshold of ≥ 30% DV
Prepackaged products with a reference amount > 30 g or 30 mL other than main dishes: threshold of ≥ 15% DV
In this example, the applicable % DV threshold is ≥ 30% DV given that lasagna is a main dish with a reference amount ≥ 200 g.
Determine the amount of saturated fat, sugars and sodium in the base quantity of the food.
Convert the saturated fat, sugars and sodium content declared per serving size in the NFt into content per reference amount. The following formula could be used: (Nutrient content per serving size / Serving size) x Reference amount = Nutrient content per reference amount.
The nutrient content per reference amount of lasagna is shown below:
Table A1.1. Nutrient content per reference amount of lasagna
Nutrient
Content per serving size declared in NFt (227 g)
Content per reference amount (300 g)
Saturated fat
5 g
6.61 g
Sugars
1 g
1.32 g
Sodium
580 mg
766.52 mg
Identify the applicable Daily Value for saturated fat, sugars and sodium.
Consult Part 1 of the Table of Daily Values and determine in which column the applicable DVs are specified based on the intended consumers identified in Step 1:
Column 2: DVs used for thresholds applicable to prepackaged products intended solely for children one to four years or
Column 3: DVs used for thresholds applicable to prepackaged products intended for children and/or adults
In this example, the applicable DVs are in column 3. They are 20 g for saturated fat and trans fat, 100 g for sugars and 2300 mg for sodium.
Determine whether the amount of saturated fat, sugars and/or sodium in the base quantity of the food meets or exceeds the threshold.
Calculate the % DV for the saturated fat, sugars and sodium content per reference amount using values calculated in Step 4 and the DV identified in Step 5.
In this example, the % DVs for the nutrient content per reference amount are shown below:
Table A1.2. % DVs for the nutrient content per reference amount
Nutrient
Content per reference amount (300 g)
Daily Value
% DV calculationFootnote 1 [(Nutrient content per reference amount/DV for the nutrient) x 100]
% DV threshold
Saturated fat
6.61 g
20 g
33.05% [(6.61 g ∕ 20 g)*100]
≥ 30%
Sugars
1.32 g
100 g
1.32% [(1.32 g ∕ 100 g)*100]
≥ 30%
Sodium
766.52 mg
2300 mg
33.47% [(770 mg ∕ 2300 mg)*100]
≥ 30%
1
There are no prescribed rounding rules for determining whether the nutrient content per reference amount meets or exceeds the applicable thresholds. However, regulated parties should apply similar rounding rules that exist for calculating the % DV declared in the NFt. In this example, the unrounded content of saturated fat and of sugars per reference amount were used for the calculation, however rounded content is also permitted. The rounded content of sodium was used in accordance with the NFt rounding rules.
Compare the % DV calculated for each nutrient and the % DV threshold. If the calculated % DV is equal to or greater than the % DV threshold for one or more of the three nutrients, a symbol for the nutrient or nutrients is required.
In this example, the % DV for the saturated fat and sodium content per reference amount of lasagna meet or exceed the 30% DV threshold. Therefore, the label must carry a symbol for "high in sat fat and sodium".
See the Presentation section for more information on the symbol location and presentation requirements.
Example D – the food requires preparation and has a reference amount for its unprepared form
This example illustrates a scenario in which the prepackaged product is sold in its unprepared form. In other words, it either needs to be reconstituted with water (or other liquid) or combined with another ingredient and it has a reference amount for its unprepared form in the Table of Reference Amounts.
Consider chocolate cake mix. In this example, the reference amount is the amount of unprepared mix required to make 80 g of the final product because it is a medium weight cake. The serving of stated size (serving size) declared in the Nutrition Facts Table (NFt) is 1/10 of package (43 g). These instructions describe the steps to follow to determine whether the amount of saturated fat, sugars and/or sodium meets or exceeds the applicable threshold and therefore, triggers the need to display the front-of-package (FOP) nutrition symbol (the symbol) on the label.
Identify for whom the product is intended.
Determine which of the following 2 categories applies to the food:
A food intended solely for children one year of age or older, but less than four years of age (children one to four years only).
A food intended for children one year of age or older, but less than four years of age or for children four years of age or older and adults (children and/or adults).
In this example, the product is intended for children and/or adults. Therefore, the thresholds in columns 2 to 4 of the table to section B.01.350 (Thresholds Requiring a Nutrition Symbol) apply.
Identify the quantity of food that must be used to assess the amount of saturated fat, sugars and/or sodium content against the symbol threshold.
Consult the Table of Reference Amounts to identify the amount applicable to the product
The reference amount for medium weight cake mix is the amount of unprepared mix required to make 80 g prepared; it is set out in Item A.6, Column 2, of the Table of Reference Amounts.
Compare the product's reference amount and the serving size declared in the NFt. The larger quantity must be used as the base quantity for the nutrient content assessment
In this example, the serving size and reference amount are equal. Therefore, the serving size of 1/10 of package (43 g) of the unprepared product can be used as the base quantity for the assessment.
Identify the applicable % Daily Value (% DV) threshold.
Determine in which of the following classes the product belongs:
Prepackaged products with a reference amount ≤ 30 g or 30 mL: threshold of ≥ 10% DV
Prepackaged products with a reference amount > 30 g or 30 mL other than main dishes: threshold of ≥ 15% DV
Prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults): threshold of ≥ 30% DV
In this example, the applicable % DV threshold is ≥ 15% DV given that the reference amount for the unprepared cake mix is > 30 g or 30 mL.
Determine whether the amount of saturated fat, sugars or sodium in the base quantity of the food meets or exceeds the threshold.
When the serving size is the base quantity for the nutrient content assessment the % DV for sugars and sodium declared in the NFt can be compared to the % DV thresholds for the symbol identified in Step 3. It is important to note that the NFt presents the % DV for saturated fat andtransfat content combined and that for FOP labelling purposes, only saturated fat content must be considered when calculating the % DV to determine whether a "high in sat fat" symbol is required. If a food contains trans fat, the % DV for saturated and trans fat content declared in the NFt should not be compared to the % DV threshold for the symbol. If a food contains no trans fat, the % DV for saturated and trans fat content declared in the NFt can be compared to the threshold.
If the % DV for one or more of the nutrients is equal to or greater than the % DV threshold, a symbol for the nutrient or nutrients is required.
In this example, the % DV declared for saturated fat and trans fat in the NFt (5%) can be compared to the % DV thresholds because the food contains no trans fat
The % DV for sugars (18%) and sodium (20%) declared in the NFt were also compared to the 15% DV threshold.
In this example, the % DV for sugars and sodium meet or exceed the threshold. The label must carry a symbol for "high in sugars and sodium".
See the Presentation section for more information on the symbol location and presentation requirements.
Example E – the serving size is greater than the reference amount and the product is intended solely for children one to four years of age
This example illustrates a scenario in which the serving of stated size (serving size) declared in the Nutrition Facts table (NFt) is larger than the reference amount set out for the food in the Table of Reference Amounts and the food is intended to be consumed by young children only.
Consider toddler biscuits sold in a box. The serving size declared in the NFt is 1 biscuit (10 g). These instructions describe the steps to follow to determine whether the amount of saturated fat, sugars and/or sodium meets or exceeds the applicable threshold and therefore, triggers the need to display the front-of-package (FOP) nutrition symbol (the symbol) on the label.
Identify for whom the product is intended.
Determine which of the following 2 categories applies to the food:
A food intended solely for children one year of age or older, but less than four years of age (children one to four years only).
A food intended for children one year of age or older, but less than four years of age or for children four years of age or older and adults (children and/or adults).
In this example, the product is intended for children one to four years only. Therefore, the thresholds in columns 5 to 7 of the table to section B.01.350 (Thresholds Requiring a Nutrition Symbol) apply.
Identify the quantity of food that must be used to assess the amount of saturated fat, sugars and/or sodium against the symbol threshold.
Consult the Table of Reference Amounts to identify the amount applicable to the product.
The reference amount for biscuits for children under four years of age is 7 g; it is set out in Item W.3, Column 2, of the Table of Reference Amounts.
Compare the product's reference amount and the serving size declared in the NFt. The larger quantity must be used as the base quantity for the nutrient content assessment.
In this example, the serving size (10 g) is greater than the reference amount. Therefore, the serving size is the base quantity that must be used for the assessment.
Identify the applicable % Daily Value (% DV) threshold.
Determine in which of the following classes the product belongs:
Prepackaged products with a reference amount ≤ 30 g or 30 mL: threshold of ≥ 10% DV
Prepackaged products with a reference amount > 30 g or 30 mL other than main dishes: threshold of ≥ 15% DV
Prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults): threshold of ≥ 30% DV
In this example, the applicable threshold is ≥ 10% DV given that the biscuits have a reference amount ≤ 30 g or 30 mL.
Determine whether the amount of saturated fat, sugars and/or sodium in the base quantity of the food meets or exceeds the threshold.
When the serving size is the base quantity for the nutrient content assessment the % DV for sugars and sodium declared in the NFt can be compared to the % DV thresholds identified in Step 3. It is important to note that the NFt presents the % DV for saturated fat and trans fat content combined and that for FOP labelling purposes, only saturated fat content must be considered when calculating the % DV to determine whether a "high in sat fat" symbol is required. If a food contains trans fat, the % DV for saturated and trans fat content declared in the NFt should not be compared to the % DV threshold for the symbol. If a food contains no trans fat, the % DV for saturated and trans fat content declared in the NFt can be compared to the threshold.
If the % DV for one or more of the nutrients is equal to or greater than the % DV threshold, a symbol for the nutrient or nutrients is required.
In this example, the % DV declared for saturated and trans fat in the NFt (0%) can be compared to the % DV thresholds because the food contains no trans fat
The % DV for sugars (6%) and sodium (2%) declared in the NFt were also compared to the 10% DV threshold.
In this example, the % DV for all three nutrients are below the threshold. Therefore, no symbol is required on the label.
Example F – the serving size and reference amount are equal and the food has a reference amount ≤ 30 g or 30 mL
This example illustrates a scenario in which the serving of stated size (serving size) declared in the Nutrition Facts table (NFt) is equal to the reference amount for the food in the Table of Reference Amounts and the food has a reference amount of ≤ 30 mL.
Consider soy sauce sold in a bottle. The serving size declared in the NFt is 1 tbsp. (15 mL). These instructions describe the steps to follow to determine whether the amount of saturated fat, sugars and/or sodium meets or exceeds the applicable threshold and therefore, triggers the need to display the front-of-package (FOP) nutrition symbol (the symbol) on the label.
Identify for whom the product is intended.
Determine which of the following 2 categories applies to the food:
A food intended solely for children one year of age or older, but less than four years of age (children one to four years only).
A food intended for children one year of age or older, but less than four years of age or for children four years of age or older and adults (children and/or adults).
In this example, the product is intended for children and/or adults. Therefore, the thresholds in columns 2 to 4 of the table to section B.01.350 (Thresholds Requiring a Nutrition Symbol) apply.
Identify the quantity of food that must be used to assess the amount of saturated fat, sugars and/or sodium against the symbol threshold.
Consult the Table of Reference Amounts to identify the amount applicable to the product.
The reference amount for soy sauce is 15 mL; it is set out in Item R.5, Column 2, of the Table of Reference Amounts.
Compare the product's reference amount and the serving size declared in the NFt. The larger quantity must be used as the base quantity for the nutrient content assessment.
In this example, the serving size and reference amount are equal. Therefore, the serving size can be used as the base quantity for the assessment.
Identify the applicable % Daily Value (% DV) threshold.
Determine in which of the following classes the product belongs:
Prepackaged products with a reference amount ≤ 30 g or 30 mL: threshold of ≥ 10% DV
Prepackaged products with a reference amount > 30 g or 30 mL other than main dishes: threshold of ≥ 15% DV
Prepackaged main dishes with a reference amount ≥ 170 g (when intended solely for children one to four years) or ≥ 200 g (when intended for children and/or adults): threshold of ≥ 30% DV
In this example, the applicable threshold is ≥ 10% DV given that soy sauce has a reference amount ≤ 30 g or 30 mL.
Determine whether the amount of saturated fat, sugars and/or sodium in the base quantity meets or exceeds the threshold.
When the serving size is the base quantity for the nutrient content assessment the % DV for sugars and sodium declared in the NFt can be compared to the % DV thresholds identified in Step 3. It is important to note that the NFt presents the % DV for saturated fat and trans fat content combined and that for FOP labelling purposes, only saturated fat content must be considered when calculating the % DV to determine whether a "high in sat fat" symbol is required. If a food contains trans fat, the % DV for saturated and trans fat content declared in the NFt should not be compared to the % DV threshold for the symbol. If a food contains no trans fat, the % DV for saturated and trans fat content declared in the NFt can be compared to the threshold.
If the % DV for one or more of the nutrients is equal to or greater than the % DV threshold, a symbol for the nutrient or nutrients is required.
In this example, only the % DV for sodium declared in the NFt (50%) is equal to or greater than the 10% DV threshold. Therefore, the label must carry a symbol for "high in sodium".
See the Presentation section for more information on the symbol location and presentation requirements.
Appendix 2: Steps for choosing a FOP nutrition symbol format
These instructions describe steps to follow to identify the FOP nutrition symbol (the symbol) format required on the label of different prepackaged products.
Example A: general rules of application for symbol presentation
Example A – general rules of application for symbol presentation
This example illustrates a typical scenario in which the general rules of application apply.
Consider a box of granola-type breakfast cereal, for which it has been determined that the saturated fat and sugars content exceeds the thresholds (see the Thresholds section for more information). Therefore, a symbol must appear on the label to indicate that the cereal is "high in" these two nutrients.
These instructions describe the steps to follow to identify the symbol format required on the label.
Identify the product's principal display surface (PDS).
Refer to the PDS definition to determine which surface of the package is considered the PDS.
The front panel of the box of cereal is displayed under normal conditions of sale. Therefore, it is considered the PDS. In this example, the package is labelled in English on one of the two large panels. It is labelled in French on the other large panel. Either one of the larger panels could be considered the PDS. Both are included in this example.
Calculate the PDS (size).
The PDS is equal to 721 cm2. The PDS is crosshatched on both large panels of the cereal box in Figure A2.1.
Did you know? The size of the symbol is proportional to the PDS. In most cases, the larger the PDS the larger the symbol on the label.
Identify the product's principal display panel (PDP).
Refer to the PDP definition to determine which part of the label is considered the PDP. The dimensions of the PDP determine where to place the symbol and validate which symbol orientation must be used.
In this example, the PDP of the box of cereal is the same part of the label as the PDS. The PDP is shaded on both large panels of the cereal box in Figure A2.2. The shading overlaps with the crosshatching used to identify the PDS because the areas are the same part of the label.
Did you know? The symbol must appear on the PDP.
Consult the table to section B.01.352 of theFood and Drug Regulations(FDR) (Nutrition Symbols and Formats table) to identify the symbol format that must appear on the label.
Refer to Column 1 (Range of principal display surface) to determine whether the PDS calculated in Step 2 corresponds to Item 1 (> 30 cm2) or Item 2 (≤ 30 cm2).
The PDS of 721 cm2corresponds toItem 1 (> 30 cm2).
Within that item, refer to Column 2 (Nutrients that meet or exceed threshold […]) to find the "high in" nutrient combination that applies to the product.
The cereal is "high in sat fat" and "high in sugars". Therefore, the applicable combination is Saturated fat (Sat fat) and sugars.
Choose a language option (unilingual or bilingual) to determine which column sets out the applicable format: Column 3, 4, 5 or 6.
In this example, unilingual symbols are the language option used. This narrows down the relevant columns to Column 3 (Nutrition symbol in unilingual horizontal format) or 4 (Nutrition symbol in unilingual vertical format).
Validate the symbol orientation (horizontal or vertical).
The regulations set out the horizontal format as the default orientation. The vertical format is required only if the product has a PDS ≤ 450 cm2 and the horizontal format that would otherwise need to be used on the label is wider than the PDP (see the Presentation section for more information).
In this example, the PDS is larger than 450 cm2, therefore vertical symbols are not permitted. Horizontal symbols must be used. This eliminates Column 4 and means that the applicable symbol format is set out in Column 3 (Nutrition symbol in unilingual horizontal format).
Identify the symbol format that must appear on the label.
Given that:
the PDS falls within Item 1 of the table to B.01.352 of the FDR
the cereal is "high in sat fat" and "high in sugars"
the language option chosen is unilingual and
the default horizontal orientation applies
symbol formats 2(EH) and 2(FH) set out in Column 3 must be displayed on the English label and French label, respectively. Refer to Schedule K.1 of the FDR to see an image of these two formats.
Table A2.1. Excerpt from the table to section B.01.352 of the FDR
Item
Column 1 Range of principal display surface
Column 2 Nutrients that meet or exceed threshold in subsection B.01.350(1)
Column 3 Nutrition symbol in unilingual horizontal format
Column 4 Nutrition symbol in unilingual vertical format
Column 5 Nutrition symbol in bilingual horizontal format
Column 6 Nutrition symbol in bilingual vertical format
1
> 30 cm2
Saturated fat (Sat fat), sugars and sodium
1(EH) and 1(FH)
1(EV) and 1(FV)
1(BH)
1(BV)
Saturated fat (Sat fat) and sugars
2(EH) and 2(FH)
2(EV) and 2(FV)
2(BH)
2(BV)
Consult the Compendium of Nutrition Symbol Formats and associated graphic files to find the symbol that must appear on the label (refer to section 6.8 for how to obtain these documents).
Refer to the Table of Contents to identify the section with the language and symbol orientation that matches the symbol formats identified in Step 4.
In this example, the applicable section is Unilingual Horizontal Format.
Within that section, find the relevant PDS range.
In this example, the relevant range is > 600 cm2.
Within that PDS range, find the symbol with the nutrient combination that applies to the product.
In this example, the relevant symbols are Figures 1.2(EH) and 1.2(FH).
Find the appropriate .EPS graphic files in the package.
Did you know? Different naming conventions are used to identify a given symbol format in the regulations and in the Compendium of Nutrition Symbol Formats. Appendix A in the Compendium shows how these different conventions align.
Determine where to place the symbol on the label.
Compare the height and width of the PDP to determine whether the symbol must appear in the upper half (50%) or in the right half (50%) of the PDP.
In this example, the height of the PDP is greater than the width. Therefore, the symbol must be placed in the upper half (50%) of the PDP (see the Presentation section for more information).
Consult the Directory of Nutrition Symbol Specifications to determine the dimension of the buffer surrounding the symbols.
There must be a buffer zone around the symbol without any text or other graphic material.
Refer to the Table of Contents to identify the table with the language and symbol orientation that matches the symbol formats identified in Step 4.
In this example, the relevant table is Table 1 - Unilingual Horizontal Format.
Within that table, refer to Column 1 to identify the relevant PDS range.
In this example, the relevant PDS range is > 600 cm2.
Within that PDS range, refer to Column 4 to identify the minimum buffer dimension required.
In this example, the minimum buffer dimension is 2.7 mm.
Table A2.2. Excerpt of Table 1 from the Directory of Nutrition Symbol Specifications of the FDR
Table 1 Unilingual Horizontal Format
Item
Column 1 Range of principal display surface
Column 2 Nutrition symbol in Schedule K.1 of the Food and Drug Regulations
Column 3 Nutrition symbol dimensions (width x height)
Column 4 Minimum buffer surrounding the nutrition symbol
Column 5 Height of upper case letters or tallest ascender of lower case letters (except for the words Health Canada / Santé Canada)
Column 6 Height of upper case letters or tallest ascender of lower case letters for the words Health Canada / Santé Canada
Column 7 "x" height of letters (except for the words Health Canada / Santé Canada)
Column 8 "x" height of letters for the words Health Canada / Santé Canada
Column 9 Height of the black / white bars
Column 10 Diameter of the lens of the magnifying glass
1
> 600 cm2
1(EH) and 1(FH)
2(EH) and 2(FH)
3(EH) and 3(FH)
4(EH) and 4(FH)
5(EH) and 5(FH)
6(EH) and 6(FH)
7(EH) and 7(FH)
4.42 cm x 3.30 cm
2.7 mm
3.5 mm
3.0 mm
2.7 mm
2.3 mm
6.2 mm
17.3 mm
Example B – required use of a vertical symbol
This example illustrates a scenario where the use of a vertical symbol is assessed and determined to be required.
Consider a bottle of juice for which it has been determined that the sugars content exceeds the threshold (see the Thresholds section for more information). Therefore, a symbol must appear on the label to indicate that the juice is "high in sugars".
These instructions describe the steps to follow to identify the symbol format required on the label.
Identify the product's principal display surface (PDS).
Refer to the PDS definition to determine which surface of the package is considered the PDS.
The entire front of the bottle is displayed under normal conditions of sale. Therefore, it is considered the PDS.
Calculate the PDS (size).
The PDS is equal to 158 cm2. The PDS is crosshatched on the juice bottle in Figure A2.4.
Identify the product's principal display panel (PDP).
Refer to the PDP definition to determine which part of the label is considered the PDP. The dimensions of the PDP determine where to place the symbol and validate which symbol orientation must be used.
In this example, the PDP of the bottle is the part of the label that is applied to the PDS. The PDP is shaded on the bottle of juice in Figure A2.5. The shading overlaps with the crosshatching used to identify the PDS because the PDP covers a portion of the PDS.
Consult the table to section B.01.352 of theFood and Drug Regulations(FDR) (Nutrition Symbols and Formats table) to identify the applicable nutrition symbol format.
Refer to Column 1 (Range of principal display surface) to determine whether the PDS calculated in Step 2 corresponds to Item 1 (> 30 cm2) or Item 2 (≤ 30 cm2).
The PDS of 158 cm2 corresponds to Item 1 (> 30 cm2).
Within that item, refer to Column 2 (Nutrients that meet or exceed threshold […]) to find the "high in" nutrient combination that applies to the product.
The juice is "high in sugars". Therefore, the applicable combination in Column 2 is Sugars.
Choose a language option (unilingual or bilingual) to determine which column sets out the applicable format: Column 3, 4, 5 or 6.
In this example, a bilingual symbol (with English text shown first) is used as the language option. This narrows down the relevant columns to Column 5 (Nutrition symbol in bilingual horizontal format) or 6 (Nutrition symbol in bilingual vertical format).
Validate the symbol orientation (horizontal or vertical).
The regulations set out the horizontal format as the default orientation. The vertical format is required only if the product has a PDS ≤ 450 cm2 and the horizontal format that would otherwise need to be used on the label is wider than the PDP (see the Presentation section for more information).
The PDS of this product is < 450 cm2, therefore it is relevant to compare the width of the horizontal symbol and the width of the PDP to determine whether a vertical symbol must be used.
First, identify the symbol format in the default horizontal orientation.
Given that:
the PDS falls within Item 1 of the table to B.01.352 of the FDR
the juice is "high in sugars" and
the language option chosen is bilingual
symbol format 6(BH) set out in Column 5 is the format in the default horizontal orientation.
Table A2.3. Excerpt from the table to section B.01.352 of the FDR
Item
Column 1 Range of principal display surface
Column 2 Nutrients that meet or exceed threshold in subsection B.01.350(1)
Column 3 Nutrition symbol in unilingual horizontal format
Column 4 Nutrition symbol in unilingual vertical format
Column 5 Nutrition symbol in bilingual horizontal format
Column 6 Nutrition symbol in bilingual vertical format
1
> 30 cm2
Saturated fat (Sat fat), sugars and sodium
1(EH) and 1(FH)
1(EV) and 1(FV)
1(BH)
1(BV)
Sugars
6(EH) and 6(FH)
6(EV) and 6(FV)
6(BH)
6(BV)
Next, consult the Directory of Nutrition Symbol Specifications to find the width of the horizontal symbol. Refer to the Table of Contents to identify the table with the applicable language option in the horizontal orientation.
In this example, the language option is bilingual. Therefore, the relevant table is Table 3 - Bilingual Horizontal Format.
Within that table, refer to Column 1 to identify the relevant PDS range.
In this example, the relevant PDS range is > 100 cm2 to ≤ 250 cm2.
Within that PDS range, refer to Column 3 to find the width of the symbol in the default horizontal orientation.
In this example, the width of the horizontal symbol (that is, format 6(BH)) is 3.60 cm.
Table A2.4. Excerpt of Table 3 from the Directory of Nutrition Symbol Specifications of the FDR
Table 3 Bilingual Horizontal Format
Item
Column 1 Range of principal display surface
Column 2 Nutrition symbol in Schedule K.1 of the Food and Drug Regulations
Column 3 Nutrition symbol dimensions (width x height)
Column 4 Minimum buffer surrounding the nutrition symbol
Column 5 Height of upper case letters or tallest ascender of lower case letters (except for the words Health Canada / Santé Canada)
Column 6 Height of upper case letters or tallest ascender of lower case letters for the words Health Canada / Santé Canada
Column 7 "x" height of letters (except for the words Health Canada / Santé Canada)
Column 8 "x" height of letters for the words Health Canada / Santé Canada
Column 9 Height of the black / white bars
Column 10 Diameter of the lens of the magnifying glass
4
> 100 cm2 to ≤ 250 cm2
1(BH)
2(BH)
3(BH)
4(BH)
5(BH)
6(BH)
7(BH)
3.60 cm x 1.89 cm
1.5 mm
2.0 mm
1.8 mm
1.5 mm
1.3 mm
3.5 mm
9.9 mm
Compare the width of the PDP and the width of the symbol in the default horizontal orientation to determine whether the vertical orientation must be used.
In this example, the width of symbol 6(BH) is greater than the width of the PDP. Therefore, the vertical orientation must be used on the label.
This eliminates Column 5 and means that the vertical symbol format set out in Column 6 (Nutrition symbol in bilingual vertical format) of the table to B.01.352 of the FDR must be used on the label. In this example, the applicable symbol in the vertical orientation is format 6(BV). Refer to Schedule K.1 of the FDR to see an image of this format.
Consult the Compendium of Nutrition Symbol Formats and associated graphic files to find the symbol that must appear on the label (refer to section 6.8 for how to obtain these documents).
Refer to the Table of Contents to identify the section with the language and symbol orientation that matches the symbol format identified in Step 4.
In this example, the applicable section is Bilingual Vertical Format.
Within that section, find the relevant PDS range.
In this example, the relevant range is > 100 cm2 to ≤ 250 cm2.
Within that PDS range, find the symbol with the applicable nutrient combination.
In this example, the relevant symbol is Figure 4.6(BV).
Find the appropriateness graphic file in the package.
Determine where to place the symbol on the label.
Compare the height and width of the PDP to determine whether the symbol must appear in the upper half (50%) or in the right half (50%) of the PDP.
In this example, the height of the PDP is greater than the width. Therefore, the symbol must be placed in the upper half (50%) of the PDP (see the Presentation section for more information).
Consult the Directory of Nutrition Symbol Specifications to determine the dimension of the buffer surrounding the symbol.
There must be a buffer zone around the symbol without any text.
Refer to the Table of Contents to identify the table with the language and symbol orientation that matches the symbol format identified in Step 4.
In this example, the relevant table is Table 4 - Bilingual Vertical Format.
Within that table, refer to Column 1 to find the relevant PDS range.
In this example, the relevant range is > 100 cm2 to ≤ 250 cm2.
Within that PDS range, refer to Column 4 to identify the minimum buffer dimension required.
In this example, the minimum buffer dimension required is 1.5 mm.
Table A2.5. Excerpt of Table 4 from the Directory of Nutrition Symbol Specifications of theFood and Drug Regulations
Table 4 Bilingual Vertical Format
Item
Column 1 Range of principal display surface
Column 2 Nutrition symbol in Schedule K.1 of the Food and Drug Regulations
Column 3 Nutrition symbol dimensions (width x height)
Column 4 Minimum buffer surrounding the nutrition symbol
Column 5 Height of upper case letters or tallest ascender of lower case letters (except for the words Health Canada / Santé Canada)
Column 6 Height of upper case letters or tallest ascender of lower case letters for the words Health Canada / Santé Canada
Column 7 "x" height of letters (except for the words Health Canada / Santé Canada)
Column 8 "x" height of letters for the words Health Canada / Santé Canada
Column 9 Height of the black / white bars
Column 10 Diameter of the lens of the magnifying glass