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Morevaping was warned for offering electronic nicotine delivery system (ENDS) products for sale on its website without obtaining required premarket authorization orders, in violation of the Federal Food, Drug, and Cosmetic Act. The FDA determined that the company's products qualify as tobacco products subject to FDA jurisdiction because they contain nicotine from any source and are intended for human consumption, requiring compliance with new tobacco product regulations. The company failed to secure the legally mandated marketing authorization orders under section 910 of the FD&C Act, which are required for any tobacco product not commercially marketed in the United States prior to February 15, 2007.