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