Big News: FDA is moving from MasterControl to ComplianceQuest.See Why
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Talk to a SpecialistTalk to a SpecialistThe FDA's Center for Tobacco Products determined that tendollarvapes.com was offering electronic nicotine delivery system (ENDS) products for sale without proper premarket authorization as required under the Family Smoking Prevention and Tobacco Control Act. The company failed to comply with FDA requirements that "new tobacco products"—including vaping products containing nicotine from any source—must obtain a marketing authorization order before being legally marketed in the United States. This violation applied to ENDS products listed on the company's website that were not commercially marketed in the U.S. prior to February 15, 2007, or were modified versions marketed after that date.