About FDA
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What products are considered to be tobacco products as defined by the tobacco control act?
The term "tobacco product" means any product made or derived from tobacco that is intended for human consumption, including any component, part, or accessory of a tobacco product. This includes, among other products, cigarettes, cigarette tobacco, roll-your-own tobacco, and smokeless tobacco.
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- FDA Center for Tobacco Products Inaugural Year and Looking Forward
- FDA Basics Webinar: State Enforcement Program
- Is FDA going to ban tobacco?
- What will FDA do to curb tobacco use among children and adolescents?
- What are some of the key regulatory timelines associated with the tobacco control act?
- How does FDA plan to enforce the restrictions on promotion and advertising established by the Tobacco Control Act?
- What Should I Do If I See Violations of FDA’s Tobacco Products Rules?
- What are FDA’s Regulations for Flavored Tobacco?
- What are the new Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children and Adolescents?
- How does the regulation of tobacco products differ from FDA’s regulation of drugs or medical devices?
- What is the main goal in regulating tobacco products?
- What are the priorities of the Center for Tobacco Products?
- What part of FDA regulates tobacco products?
- What products are not considered to be tobacco products as defined by the tobacco control act?
- What products are considered to be tobacco products as defined by the tobacco control act?
- Does FDA have the authority to regulate tobacco products?
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