| Literature DB >> 28071877 |
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Abstract
The 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 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.Entities:
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Year: 2017 PMID: 28071877
Source DB: PubMed Journal: Fed Regist ISSN: 0097-6326