SUBCHAPTER IX— TOBACCO PRODUCTS
Sections
- § 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