FD&C
FDA Warns Selling of Topical CBD Products Violates FD&C Act
On March 22, the U.S. Food and Drug Administration stated that it has issued warning letters to two companies for selling topical pain relief products labeled as containing cannabidiol (CBD) in ways that violate the Federal Food, Drug, and Cosmetic Act (FD&C Act). Specifically, the warning letters addressed the illegal marketing of unapproved drugs labeled […]
NPA Comments on EPA’s Standards for Hazardous Waste Pharmaceuticals
The Natural Products Association (NPA) submitted comments regarding the Environmental Protection Agency’s (EPA) proposed rule under the Resource Conservation and Recovery Act (RCRA) – “Management Standards for Hazardous Waste Pharmaceuticals.” In its comments, NPA requested EPA to reevaluate the inclusion of dietary supplements under the definition of pharmaceuticals in its hazardous waste proposed rule. NPA […]
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