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Food, Drug, and Cosmetic Act

The United States Federal Food, Drug, and Cosmetic Act (FFDCA, FDCA, or FD&C) is a set of laws passed by Congress that give the Food and Drug Administration (FDA) authority to oversee the safety of food, drugs, medical devices, and cosmetics. The FDCA is located in the United States Code, beginning at 21 U.S.C. §301.

In Minnesota, as in all states, the Federal Food, Drug, and Cosmetic Act (FDCA) provides the framework for the regulation of food, drugs, medical devices, and cosmetics. This federal law, which is found in Title 21 of the United States Code starting at Section 301, grants the Food and Drug Administration (FDA) the authority to ensure that these products are safe for public use and are properly labeled. The FDA's regulations are nationally applicable, including in Minnesota, and the state's agencies and regulatory bodies work in conjunction with the FDA to enforce these standards. The FDCA prohibits the interstate commerce of products that are adulterated or misbranded, and it outlines the processes for premarket approval of drugs and medical devices, as well as the safety standards for food and cosmetics. Minnesota businesses and consumers must adhere to the FDCA, along with any relevant state statutes that may provide additional regulations on these products.

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Consumers

Food, Drug, and Cosmetic Act

As a LegalFix Member You Will Be an Important Client of Local Law Firms

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Minnesota State Code

Minnesota State Code

Consumers

Food, Drug, and Cosmetic Act

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