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Juice Man LLC was cited for manufacturing and selling e-liquid tobacco products without required premarket authorization. The FDA determined that the company's e-liquid products, which contain nicotine from tobacco or other sources, are subject to FDA jurisdiction as tobacco products under the Federal Food, Drug, and Cosmetic Act and must comply with all applicable regulations. The company failed to obtain premarket authorization orders before marketing these "new tobacco products" that were not commercially available in the United States as of February 15, 2007.