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Free Range Vapor LLC was warned that its e-liquid products sold through its website were deemed tobacco products subject to FDA regulation under the Family Smoking Prevention and Tobacco Control Act, but lacked required premarket authorization orders for new tobacco products. The company failed to comply with Federal Food, Drug, and Cosmetic Act requirements applicable to e-liquids, which have been subject to FDA jurisdiction since August 8, 2016. The FDA determined that the e-liquids were being manufactured and distributed for sale in the United States without the legally required marketing authorization before their commercial distribution.