Subchapter IX — Tobacco Products
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- §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