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High Light Vape Co. was warned for offering electronic nicotine delivery system (ENDS) products for sale without required premarket authorization, in violation of the Federal Food, Drug, and Cosmetic Act. The FDA determined that products listed on the company's website were tobacco products subject to FDA jurisdiction under section 901(b) of the FD&C Act, requiring compliance with premarket approval requirements for new tobacco products. The warning emphasized that as of March 15, 2022, FDA jurisdiction expanded to include all products containing nicotine from any source, not just tobacco-derived nicotine, making the company's ENDS products subject to these regulatory requirements regardless of nicotine source.