FDA's Center for Tobacco Products regulates the manufacturing, marketing, and distribution of tobacco products to protect public health. Contact CTP 1-877-287-1373 (9am - 4pm ET)

Tobacco comes in many forms, from cigars and cigarettes to smokeless tobacco and dissolvable nicotine products. FDA works to reduce the use of these products, and the harm that they cause.

As part of its goal to improve public health and protect future generations from the risks of tobacco use, the FDA has extended its authority to cover all tobacco products.

FDA launched the Searchable Tobacco Products Database, a new user-friendly list of tobacco products—including e-cigarettes—that may be legally marketed in the United States.

2023年3月17日 · FDA's Center for Tobacco Products, which regulates tobacco products to protect public health, defines terms used in its regulations and guidances.

2024年8月21日 · Non-combusted products - such as e-cigarettes and other smokeless tobacco products - generally have lower health risks than cigarettes and other combustible tobacco products.

2023年3月17日 · Section 101 of the Tobacco Control Act defines tobacco products and lists amendments to the Federal Food, Drug, and Cosmetic Act.

What Is a Tobacco Product Standard? What Are the Family Smoking Prevention and Tobacco Control Act Special Rules? What Is the Process for Developing a Product Standard?

2024年12月16日 · There are three pathways to market a tobacco product: premarket tobacco applications (PMTA), substantial equivalence (SE), and exemption from SE.

2024年3月28日 · FDA oversees all pathways to legally market tobacco products, including applications for Substantial Equivalence (SE), Exemption from SE, and PMTA.