FDA Denies Marketing of Logic’s Menthol E-Cigarette Products
FDA denies marketing of Logic’s menthol e-cigarette products following determination they do not meet public health standard.
FDA, DOJ Seek Injunctions Against Six E-cig Manufacturers
Defendants illegally manufactured and sold unauthorized e-cigarette products even after FDA warned the companies they were violating the law.
FDA Completes Initial Review of 95% of Non-Tobacco Nicotine Product Applications
The agency has also issued a total of over 60 warning letters to manufacturers, including for products with a submitted application and negative action.
Tobacco Product Marketing Orders
To legally market a new tobacco product, manufacturers must submit an application to FDA and receive a marketing authorization from FDA. When a new tobacco product is granted a marketing order, information is posted online for public awareness. FDA notes that in accordance with a court order, deemed new tobacco products that were on the market as of August 8, 2016 were required to submit an application to FDA by September 9, 2020 or risk enforcement.Learn More About the Latest Marketing Decisions
Regulation and Enforcement of Non-Tobacco Nicotine (NTN) Products
A new federal law gives FDA the authority to regulate tobacco products containing nicotine from any source. This law took effect April 14, 2022, and after July 13, 2022, any new non-tobacco nicotine (NTN) product that has not received premarket authorization from FDA cannot be legally marketed. FDA launched a webpage that includes up-to-date information about premarket review progress and compliance and enforcement actions.Learn more
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