On June 24, 2025, the U.S. Food and Drug Administration (FDA) sent out a reminder that twice every year – by June 30 and Dec. 31 – registered tobacco product manufacturers are required to report to FDA their tobacco product listings if they have made certain changes. Information previously submitted to FDA should not be resubmitted. If a manufacturer made any of the following changes, they must be reported:

• Introduced any tobacco products for commercial distribution that were not included in a previous listing;
• Discontinued manufacturing, preparation, compounding, or processing any tobacco products for commercial distribution;
• Resumed manufacturing, preparation, compounding or processing any tobacco products previously listed as discontinued; or
• Made any required or voluntary material change to any listing information previously submitted, such as a name, labeling, consumer information, or advertisement changes.

For resources on product listing submissions, please go to the Tobacco Registration and Product Listing - Next Generation (TRLM NG) Instructions page. Manufacturers can also read the Registration and Product Listing for Owners and Operators of Domestic Product Establishments page for more information.