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U.S. Department of Health and Human Services

CFR - Code of Federal Regulations Title 21

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The information on this page is current as of Dec 22, 2023.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER K - TOBACCO PRODUCTS
 
PART 1100TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY
 

Subpart A - Tobacco Products Subject to FDA Authority
   § 1100.1 - Scope.
   § 1100.2 - Requirements.
   § 1100.3 - Definitions.
   § 1100.5 - Exclusion from tobacco regulation.

Subpart B [Reserved]

Subpart C - Maintenance of Records Demonstrating That a Tobacco Product Was Commercially Marketed in the United States as of February 15, 2007.
   § 1100.200 - Purpose and scope.
   § 1100.202 - Definitions.
   § 1100.204 - Recordkeeping requirements.

Authority: 21 U.S.C. 371, 374, 387a(b), 387e, 387i; Pub. L. 117-103, 136 Stat. 49.
Source: 81 FR 29102, May 10, 2016, unless otherwise noted.

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