In terms of enforcement actions taken in relation to non-tobacco nicotine products, the FDA reveals that it has issued 44 warning letters to manufacturers and over 300 warning letters to retailers for violations in relation to NTN products. This includes 25 new warning letters to manufacturers of NTN products issued since Aug. 3 for marketing their products without the required premarket authorization. Most of these letters came as a result of manufacturers failing to submit applications for their NTN products. The FDA also issued new warning letters to 102 retailers for illegally selling NTN products to underage customers. To access all of the latest warning letters issued by the FDA, click here.
The FDA ended its report by recognizing the importance of keeping the public informed of its work and review of these products. To make its review process and actions taken in relation to NTN products more transparent, the agency has launched a non-tobacco nicotine product webpage that will include up-to-date information about the premarket review progress and compliance of enforcement actions. You can access that page by clicking here.
For all the latest news from the U.S. Food and Drug Administration, visit FDA.gov.
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