Tobacco Products

Clarification of When Products Made or Derived From Tobacco Are Regulated as Drugs, Devices, or Combination Products; Amendments to Regulations Regarding "Intended Uses"

21 CFR Parts 201, 801, and 1100

January 2017

The U.S. Food and Drug Administration (FDA) is issuing this final rule to describe the circumstances in which a product made or derived from tobacco, that is intended for human consumption, will be subject to regulation as a tobacco product, drug, device, or a combination product under the Federal Food, Drug, and Cosmetic Act (the FD&C Act). This action is intended to provide direction to regulated industry and to help avoid consumer confusion.


 

Page Last Updated: 01/06/2017
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