US FDA Food Labeling Regulations (21 CFR Part 101)
Subpart A: General provisions (principal display panel, information panel, identity, ingredients, name and place of business, nutrition labeling, warnings, misbranding) – US FDA Food Labeling Regulations (21 CFR Part 101)

US FDA Food Labeling Regulations (21 CFR Part 101) 101.3: Statement of identity on the PDP: the common or usual name, standardized name or descriptive name, in bold type parallel to the base, with form of the food and the 'imitation' rule (101.3)

The PDP must bear the statement of identity: the name established by law or regulation (standardized foods), the common or usual name, or an appropriately descriptive term or a fanciful name commonly used by the public where the nature is obvious, in bold type of a size reasonably related to the most prominent printed matter, in lines generally parallel to the base of the package. Where the food is marketed in different optional forms (whole, sliced, diced) the form must be shown or visible through the package. A food that stands in for and resembles another food while being nutritionally inferior must be labeled 'imitation' (101.3(e)), and a product with a standardized name must comply with that standard. Dietary supplements use the 101.3(g) statement.

Maintained by Gerard Blokdyk

Other controls in Subpart A: General provisions (principal display panel, information panel, identity, ingredients, name and place of business, nutrition labeling, warnings, misbranding) – US FDA Food Labeling Regulations (21 CFR Part 101)

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