21 CFR Part 1100
PART 1100—General
- PART 1100—General
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter K—Tobacco Products
- 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.
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