FDA Publishes Premarket Tobacco Product Application List
The Food and Drug Administration (FDA) posted on May 20 of electronic nicotine delivery system (ENDS) products for which it has received a premarket tobacco product application (PMTA) by the Sept. 9, 2020, deadline. The list includes more than 6 million products. 黑料社区has urged FDA to publish such a list so that retailers – including travel centers – will know which products are legal for them to sell. Although FDA committed to publishing a list, it was not made available until now.
On Aug. 8, 2016, all ENDS products became subject to the FDA’s tobacco authorities, including the premarket authorization requirements. This means all e-cigarettes and other ENDS products on the market at that time needed to have authorization from the FDA to be legally marketed. To remain on the market, manufacturers of ENDS products were required to submit a PMTA to FDA by Sept. 9, 2020. Once a PMTA has been submitted, a product can be sold for up to 12 months while the application is being considered.
Subscribe to Updates
The 黑料社区Foundation and 黑料社区provide a breadth of information created to strengthen travel plazas鈥� ability to meet the needs of the traveling public in an age of disruption. This includes knowledge filled blog posts, articles and publications. If you would like to receive a digest of blog post and articles directly in your inbox, please provide your name, email and the frequency of the updates you want to receive the email digest.
