Tobacco products marketed in the United States are regulated by the U.S. Food and Drug Administration (FDA). FDA’s authority extends to all tobacco products, including (but not limited to) e-cigarettes, cigars, hookah tobacco, pipe tobacco, and roll your own (RYO) tobacco.
FDA requires domestic manufacturers of tobacco products to:
- Register their establishments with FDA
- List their products with FDA (including labeling)
- Report ingredients to FDA (also applies to importers)
For assistance with U.S. FDA requirements for tobacco products, simply complete the form below: