FDA Tobacco Compliance Webinars
FDA’s Center for Tobacco Products (CTP) hosts a series of webinars on federal tobacco regulations to provide compliance education and information to retailers and small business manufacturers.
Manufacturers and Importers
The Federal Food, Drug, and Cosmetic Act (FD&C Act) defines a tobacco product manufacturer as any person, including any repacker or relabeler, who:
- Manufactures, fabricates, assembles, processes, or labels a tobacco product; or
- Imports a finished tobacco product for sale or distribution in the United States
What a Manufacturer or Vape Shop Owner Should Do After Receiving a Warning Letter (7:33)
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Retailers
It is illegal for a retailer to sell any tobacco product – including cigarettes, cigars and e-cigarettes – to anyone under 21.
After July 13, 2022, a non-tobacco nicotine product can only be legally marketed in the United States if it has received a marketing granted order (MGO) from FDA. Without this MGO, a product is in violation of the law and its manufacturer, retailer, distributor, or importer may be subject to FDA enforcement.
Language Assistance Services for Retailers Who Have Received a Tobacco CMP or NTSO Complaint (8:05)
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Part 4 – The Settlement Process for a Civil Money Penalty or a No-Tobacco Sale Order Complaint (15:24)
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Part 5 – The Hearing Process for a Civil Money Penalty or a No-Tobacco-Sale Order Complaint (17:33)
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Archived
Watch webinars from previous years: