Definition of FDA Misbranding

Definition of FDA Misbranding thumbnail
The FDA oversees food safety.

The Food and Drug Administration (FDA) ensures the safety of food, human and veterinary drugs, cosmetics, biological products, medical devices and radioactive products. One way the FDA protects public health is eliminating misbranded products.

  1. Definition

    • Misbranding occurs when a product's label is false or misleading. This includes regulations on the visibility of the product name and thorough instructions for use.

    Types

    • A package must prominently feature the product's name, manufacturer's name, required wording and an exact quantity that is inside. Instructions for use should be precise, including duration and frequency, and the suggested dosage should be safe. Labels must also comply with color additive provisions and not give the false impression of FDA approval.

    Identification

    • A company can misbrand a product by deceptive pictures, deceptive testimonials, misleading list of components and use of brand or trade names. Misbranding includes both blatantly false information and ambiguous or subjective statements.

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