Subchapter IX. Tobacco Products
Index
- 21 U.S.C. § 387 Definitions
- 21 U.S.C. § 387a Fda Authority Over Tobacco Products
- 21 U.S.C. § 387a-1 Final Rule
- 21 U.S.C. § 387b Adulterated Tobacco Products
- 21 U.S.C. § 387c Misbranded Tobacco Products
- 21 U.S.C. § 387d Submission of Health Information to the Secretary
- 21 U.S.C. § 387e Annual Registration
- 21 U.S.C. § 387f General Provisions Respecting Control of Tobacco Products
- 21 U.S.C. § 387f-1 Enforcement Action Plan For Advertising and Promotion Restrictions
- 21 U.S.C. § 387g Tobacco Product Standards
- 21 U.S.C. § 387h Notification and Other Remedies
- 21 U.S.C. § 387i Records and Reports On Tobacco Products
- 21 U.S.C. § 387j Application For Review of Certain Tobacco Products
- 21 U.S.C. § 387k Modified Risk Tobacco Products
- 21 U.S.C. § 387l Judicial Review
- 21 U.S.C. § 387m Equal Treatment of Retail Outlets
- 21 U.S.C. § 387n Jurisdiction of and Coordination With the Federal Trade Commission
- 21 U.S.C. § 387o Regulation Requirement
- 21 U.S.C. § 387p Preservation of State and Local Authority
- 21 U.S.C. § 387q Tobacco Products Scientific Advisory Committee
- 21 U.S.C. § 387r Drug Products Used to Treat Tobacco Dependence
- 21 U.S.C. § 387s User Fees
- 21 U.S.C. § 387t Labeling, Recordkeeping, Records Inspection
- 21 U.S.C. § 387u Studies of Progress and Effectiveness
- 21 U.S.C. § 387v Reporting On Tobacco Regulation Activities