U.S. Food and Drug Administration (FDA)
NPA Files Lawsuit Against FDA’s “Unlawful Application” of Food, Drug and Cosmetic Act
The Natural Products Association (NPA) filed a lawsuit on August 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 ...
Industry Criticizes Dietary Supplement Listing Act of 2024
United States Senator Dick Durbin (D-IL) introduced the Dietary Supplement Listing Act of 2024, which requires dietary supplement manufacturers to list their products with the U.S. Food and Drug Administration (FDA). In 1994, Congress passed the Dietary Supplement Health and Education Act (DSHEA), which provided FDA authority to regulate dietary supplements. However, DSHEA does not ...
Natural Grocers Supports FDA’s Ruling Against Use of Brominated Vegetable Oil
Natural Grocers by Vitamin Cottage (Lakewood, CO) announced its support for the U.S. Food and Drug Administration (FDA)’s recent revocation of the rule allowing for the use of brominated vegetable oil (BVO). The company is dedicated to improving human health, the environment and the economy and has never carried BVO products in its stores. Brominated ...
The Case of “Gas Station Heroin”
Is It Necessary for Congress to Amend the FD&C Act for FDA to Have the Authority to Prohibit Tianeptine’s Sale? If the answer to this question is “no,” why are bills being introduced into Congress to give the U.S. Food and Drug Administration (FDA) expanded authority to regulate dietary supplements? “Gas station heroin” is a ...
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