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The Center for Tobacco Products (CTP) was established by the United States Food and Drug Administration as a result of the Family Smoking Prevention and Tobacco Control Act signed by President Obama in June 2009. The FDA center was responsible for the implementation of the Family Smoking Prevention and Tobacco Control Act.

The smoking prevention and tobacco law established regulatory controls for tobacco products:

• Setting performance standards for tobacco products
• Reviewing premarket applications for new and modified risk of tobacco product
• Requirement of warning labels for tobacco products
• Enforcing advertising and promotion restrictions for tobacco products

The U.S. mandated legislation was a historic milestone for the U.S. FDA. The enacted law used to assist with the federal agency regulatory efforts and initiatives to curb the suspected health hazards for tobacco products on an annual basis.

See also

• Little Lungs in a Great Big World, public service announcement series that is part of a campaign for the CTP

References

1. "About U.S. FDA Center for Tobacco Products". Food and Drug Administration. Archived from the original on 2019-04-22. Retrieved 2019-12-16.
2. "Family Smoking Prevention and Tobacco Control Act (Public Law 111-31)" (PDF). Archived (PDF) from the original on 2011-10-16. Retrieved 2011-09-20.
3. "U.S. FDA Tobacco Products Information". Food and Drug Administration. Archived from the original on 2017-11-01. Retrieved 2019-12-16.

External links

• Official website
• Tobacco Products at FDA.gov

v t e Food and Drug Administration of the United States
Divisions	Center for Biologics Evaluation and Research Center for Devices and Radiological Health Center for Drug Evaluation and Research Center for Food Safety and Applied Nutrition Center for Tobacco Products Center for Veterinary Medicine National Center for Toxicological Research Office of Criminal Investigations Office of Global Regulatory Operations and Policy
Major acts	Family Smoking Prevention and Tobacco Control Act Modernization Act of 1997 Federal Food, Drug, and Cosmetic Act Food Safety Modernization Act Prescription Drug User Fee Act Pure Food and Drug Act
Title 21 regulations and rules	Administrative law Title 21 of the Code of Federal Regulations (CFR) Federal journal Federal Register (FR) Federal law Title 21 of the United States Code (U.S.C.)
Commissioners	Harvey W. Wiley Carl L. Alsberg Charles A. Browne Walter G. Campbell Paul B. Dunbar Charles W. Crawford George P. Larrick James L. Goddard Herbert L. Ley Charles C. Edwards Alexander M. Schmidt Donald Kennedy Jere E. Goyan Arthur H. Hayes Jr. Frank E. Young David A. Kessler Jane E. Henney Mark McClellan Lester Crawford Andrew von Eschenbach Margaret Hamburg Robert Califf Scott Gottlieb Stephen Hahn Robert Califf
Society and culture	Criticism of the Food and Drug Administration FDA Most Wanted Fugitives History of the Food and Drug Administration Regulation of food and dietary supplements by the U.S. Food and Drug Administration
Commissioner of Food and Drugs

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