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FDA Warns Selling of Topical CBD Products Violates FD&C Act

by Angela Sabarese | March 26, 2021

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 ...

FDA Issues CBD Warning Letters

by Nicholas Saraceno | December 2, 2019

The U.S. Food and Drug Administration (FDA) recently issued warning letters to 15 companies for illegally selling products containing cannabidiol (CBD) in ways that violate the Federal Food, Drug, and Cosmetic Act (FD&C Act), according to the agency. The FDA also published a revised Consumer Update detailing safety concerns about CBD products more broadly. Based on the ...

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