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Tobacco Products

FDA’s Center for Tobacco Products (CTP) works to ensure a healthier life for every family.

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Latest Updates from the Center for Tobacco Products

SE and PMTA Final Rules

FDA Issues Final Rules for PMTA and SE

These foundational rules provide additional information on the minimum requirements for PMTAs and SE Reports reviewed by FDA.
FDA Warns E-Liquid Manufacturers that did not submit premarket applications by Sept. 9 Deadline

FDA Warns Firms for Illegally Marketing Unauthorized E-liquids 

FDA issued warning letters to 10 firms that have not submitted premarket applications to the FDA and are continuing to sell or distribute unauthorized ENDS after the Sept. 9, 2020 deadline.
Seizure of 33,681 unauthorized units of e-cigarettes worth $719,453.

CBP & FDA Seize Counterfeit, Unauthorized E-Cigarettes

Joint effort demonstrates commitment to prioritizing enforcement of e-cigs most appealing and accessible to youth.
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CTP_Sept9

September 9, 2020 Premarket Review Submission Deadline

FDA created a new webpage to provide manufacturers and importers with a single location for information and resources related to tobacco product applications for deemed new tobacco products, which were due by September 9, 2020. For tips, resources, and the latest information specific to these applications, visit the new webpage.

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Tobacco 21

In December 2019, the President signed legislation raising the federal minimum age for sale of tobacco products from 18 to 21 years. Effective immediately, this law makes it illegal for a retailer to sell any tobacco product—including cigarettes, cigars, and e-cigarettes—to anyone under 21. FDA has developed a webpage to provide the latest information on this new legislation—commonly referred to as “Tobacco 21” or “T21.” The webpage currently houses responses to commonly asked questions, a recently released webinar, CTP’s web statement on the new legislation, as well as information on resources for retailers to help verify the age of customers.

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Market a Tobacco Product

New tobacco products may not be legally marketed in the U.S. without authorization from FDA. Learn more about the three pathways (SE, PMTA and EX) to market.

Small Businesses Assistance

CTP’s Office of Small Business Assistance is available to help industry understand and comply with FDA’s tobacco laws and regulations.

About the Center

FDA's Center for Tobacco Products regulates the manufacturing, marketing, and distribution of tobacco products to protect public health.

Food and Drug Administration at White Oak

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

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