The new regulations of FDA on nutrition labeling
I. nutrition labeling
the nutrition labeling and Guidance Act, which is based on the food, drugs and Cosmetics Act, requires most foods to be labeled with nutrition, and requires food labels to include nutrition ingredient statements and appropriate health statements in accordance with specific requirements
the Dietary Supplement Health Education Act requires manufacturers to add the words "dietary supplement" to product labels
although the requirements for nutrition labeling of dietary supplements and traditional foods are very different, some requirements apply to both. For example, traditional food and dietary supplements must indicate the amount of each intake of each of the 14 dietary ingredients. These 14 dietary ingredients have a specified daily intake reference amount or daily reference amount. The label must also indicate the daily intake reference amount or daily reference amount, and adopt the same format as each intake
fda has extremely detailed and strict requirements for nutrition labels (whether food or dietary supplements), and the location, area, font, size, and special marks of each item on the label are specified. For food, it is required to have a "nutrition facts" panel, and for dietary supplements, it is required to have a "supplement facts" panel. The effective content of 14 ingredients and all ingredients are required to be marked on the panel. The 14 ingredients that must be marked for the wide impact of the packaging bag are: calories, calories from fat, total fat, saturated fat, cholesterol, total sugar, food fiber, sucrose, protein, vitamin A, vitamin C, calcium, iron, sodium. (ingredients with content lower than the exempted amount are not marked)
II. Statement
① nutrition content statement. Clarify the nutritional level of the food or dietary supplement. For example, a supplement containing at least 12m g vitamin C per unit dose can be labeled "an excellent source of vitamin C"
② the health statement must be approved by FDA after reviewing the scientific literature before it can be used as a reference for dietary supplements. Currently, FDA has approved only 11 health declarations
③ nutritional support statement. One is to describe the relationship between the lack of certain nutrients and certain diseases. For example, the label of vitamin C can indicate that the lack of this ingredient will lead to scurvy. In the United States, "lack of certain nutrients" appears with similar explanations. The second is the so-called "structure function" statement
5 structure function statement. Describe the effect of total ingredients on the structure or function of a specific body, or what kind of health state can be obtained by consuming dietary supplements of the food. Like all label statements, the structure function statement must be true and non misleading
⑤ negative statement. The structure function statement label of the product must contain the following negative statement of FDA: "the statement has not been evaluated by FDA, and the product is not intended to diagnose, treat, cure or prevent any disease."
note: the nutritional support statement does not need to be approved by FDA. If the manufacturer plans to use the structure function statement on a specific product, they must notify FDA no later than 30 days after the first marketing of the product to explain their use of such statement. (Wang Yilin)
I. nutrition labeling
the nutrition labeling and Guidance Act, which is formulated on the basis of the food, drugs and Cosmetics Act, requires most foods to be labeled with nutrition labels, and requires food labels to include nutrition ingredient statements and appropriate health statements according to specific requirements
the Dietary Supplement Health Education Act requires manufacturers to add the words "dietary supplement" to product labels
although the requirements for dietary supplements and the traditional food mailbox: ang@ labeling nutrition are very different, some requirements apply to both. For example, traditional food and dietary supplements must indicate the amount of each intake of each of the 14 dietary ingredients. These 14 dietary ingredients have a specified daily intake reference amount or daily reference amount. The label must also indicate the daily intake reference amount or daily reference amount, and adopt the same format as each intake
fda has extremely detailed and strict requirements for nutrition labels (whether food or dietary supplements), and the location, area, font, size, and special marks of each item on the label are specified. For food, it is required to have a "nutrition facts" panel, and for dietary supplements, it is required to have a "supplement facts" face. The new lightweight pet aerogel is coated with a flame retardant rear panel. The effective content of 14 ingredients and all ingredients are required to be marked on the panel. The 14 ingredients that must be indicated are: calories, calories from fat, total fat, saturated fat, cholesterol, total sugar, food fiber, sucrose, protein, vitamin A, vitamin C, calcium, iron, sodium. (ingredients with content lower than the exempted amount are not marked)
II. Statement
① nutrition content statement. Clarify the nutritional level of the food or dietary supplement. For example, a supplement containing at least 12mg vitamin C per unit dose can be labeled as "an excellent source of vitamin C"
② the health statement must be approved by FDA after reviewing the scientific literature before it can be used as a reference for dietary supplements. Currently, FDA has approved only 11 health declarations
③ nutritional support statement. One is to describe the relationship between the lack of certain nutrients and certain diseases. For example, the label of vitamin C can indicate that the lack of this ingredient will lead to scurvy. In the United States, "lack of certain nutrients" appears with similar explanations. The second is the so-called "structure function" statement
5 structure function statement. Describe the effect of total ingredients on the structure or function of a specific body, or what kind of health state can be obtained by consuming dietary supplements of the food. Like all label statements, the structure function statement must be true and non misleading
⑤ negative statement. The structure function statement label of the product must contain the following negative statement that FD product maintains the high transmittance a of polycarbonate itself: "this statement has not been evaluated by FDA, and the product is not intended to diagnose, treat, cure or prevent any disease."
note: the nutritional support statement does not need to be approved by FDA. If the manufacturer plans to use the structure function statement on a specific product, they must notify FDA no later than 30 days after the first marketing of the product to explain their use of such statement
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