Food Drug and Cosmetic Act
FDA Issues Letter on DSHEA Disclaimer Amendment, Industry Responds
On Dec. 11, the U.S. Food and Drug Administration (FDA) published a letter to the dietary supplement industry regarding the agency’s labeling regulations that govern the placement of the disclaimer on dietary supplements labels under the Federal Food, Drug and Cosmetic Act (FD&C) and Dietary Supplement Health and Education Act of 1994 (DSHEA). The agency ...
FDA Declares NMN Lawful in Dietary Supplements, Industry Reacts
The U.S. Food and Drug Administration (FDA) has reversed course and confirmed that Beta (β) Nicotinamide Mononucleotide (NMN) is lawful for use in dietary supplements. Responding to citizen petitions filed by the Natural Products Association (NPA), Council for Responsible Nutrition (CRN), and the Alliance for Natural Health (ANH), the FDA revised its interpretation of a ...
NPA Wins Legal Victory Against FDA on NMN
On Nov. 5, a federal court issued a significant ruling in a lawsuit brought by the Natural Products Association (NPA) against the Food and Drug Administration (FDA) requesting that the agency cease its unlawful retroactive application of the Food, Drug and Cosmetic Act against nicotinamide mononucleotide (NMN). The court granted NPA’s request and issued a ...
NPA Files Lawsuit Against FDA’s “Unlawful Application” of Food, Drug and Cosmetic Act
The Natural Products Association (NPA) filed a lawsuit on Aug. 28 against the U.S. Food and Drug Administration (FDA), requesting the agency cease its “unlawful retroactive application” of the Food, Drug and Cosmetic Act against nicotinamide mononucleotide (NMN). “We are extremely grateful for the leadership shown by our organization’s members in deciding to take this ...
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