Tobacco Products
FDA’s Center for Tobacco Products (CTP) works to ensure a healthier life for every family.
Latest Updates from the Center for Tobacco Products
![FDA Updates Regulatory Documents to Include NTN Products](https://public4.pagefreezer.com:443/content/FDA/26-04-2023T12:46/https://www.fda.gov/files/styles/medium_3/public/2023-01-04-WEB-WEB-DefineTP%20copy%20%281%29.png?itok=mqEc0gUR)
FDA Updates Regulatory Documents to Include “Non-Tobacco Nicotine” Products
FDA will update its definition of “tobacco product” in its existing regulations and guidances to now include products that contain nicotine from any source.
![FDA denies marketing of Vuse Solo Menthol](https://public4.pagefreezer.com:443/content/FDA/26-04-2023T12:46/https://www.fda.gov/files/styles/medium_3/public/202303-BNR-Vuse_PMTA.png?itok=7LvrJjbh)
FDA Denies Marketing of Vuse Solo Menthol Products
FDA determined that Vuse Solo’s menthol-flavored e-liquid cartridges do not meet the public health standard and the products cannot be marketed.
![Modified Risk Granted Order image](https://public4.pagefreezer.com:443/content/FDA/26-04-2023T12:46/https://www.fda.gov/files/styles/medium_3/public/MRTP_1600x900.jpg?itok=tPalVyky)
FDA Authorizes Copenhagen Classic Snuff as an MRTP
Product may be marketed with: "IF YOU SMOKE, CONSIDER THIS: Switching completely to this product from cigarettes reduces risk of lung cancer."
![man in retail vape store talking with customer](https://public4.pagefreezer.com:443/content/FDA/26-04-2023T12:46/https://www.fda.gov/files/styles/call_to_action_992x558/public/CTP%20-%20Requirements%20for%20Products%20-%20Vape%20Store.jpg?itok=YlrJDjTI)
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![CTP - Actions to Address Recommendations from the Reagan-Udall Evaluation of CTP - Main Page](https://public4.pagefreezer.com:443/content/FDA/26-04-2023T12:46/https://www.fda.gov/files/styles/call_to_action_992x558/public/CTP%20-%20Actions%20to%20Address%20Recommendations%20from%20the%20Reagan-Udall%20Evaluation%20of%20CTP%20-%20Main%20Page.jpg?itok=VQgY_Lkq)
Actions to Address Recommendations from the Reagan-Udall Foundation Evaluation
At the request of FDA Commissioner Dr. Robert Califf, an independent expert panel facilitated by the Reagan-Udall Foundation (RUF) conducted an operational evaluation of CTP. A final report from the RUF evaluation included 15 recommendations, and in February 2023, CTP published a webpage with detailed plans to address each of the recommendations as quickly as possible. This webpage will be updated routinely to reflect CTP’s latest progress.
Learn About CTP’s Actions to Address the RUF Evaluation![Food and Drug Administration at White Oak](https://public4.pagefreezer.com:443/content/FDA/26-04-2023T12:46/https://www.fda.gov/files/styles/call_to_action_992x558/public/DrupalContactCTPImage.jpg?itok=bfSFaZUJ)
Contact CTP
1-877-287-1373 (9am - 4pm ET)
For General Inquiries: AskCTP@fda.hhs.gov
Center for Tobacco Products
Food and Drug Administration
10903 New Hampshire Avenue
Document Control Center
Building 71, Room G335
Silver Spring, MD 20993-0002