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Ecig Charleston LLC was warned for manufacturing and distributing e-liquid tobacco products without required premarket authorization from the FDA. The company failed to comply with the Family Smoking Prevention and Tobacco Control Act by marketing these nicotine-containing products without obtaining a marketing authorization order, which is mandatory for "new tobacco products" under section 910 of the Federal Food, Drug, and Cosmetic Act. The FDA's inspection determined that the company's e-liquid products—whether containing nicotine derived from tobacco or from other sources—were subject to FDA jurisdiction but lacked the legally required premarket approval to remain in U.S. commerce.