Subchapter IX - TOBACCO PRODUCTS
- Section 387 - Definitions
- Section 387a - FDA authority over tobacco products
- Section 387a-1 - Final rule
- Section 387b - Adulterated tobacco products
- Section 387c - Misbranded tobacco products
- Section 387d - Submission of health information to the Secretary
- Section 387e - Annual registration
- Section 387f - General provisions respecting control of tobacco products
- Section 387f-1 - Enforcement action plan for advertising and promotion restrictions
- Section 387g - Tobacco product standards
- Section 387h - Notification and other remedies
- Section 387i - Records and reports on tobacco products
- Section 387j - Application for review of certain tobacco products
- Section 387k - Modified risk tobacco products
- Section 387l - Judicial review
- Section 387m - Equal treatment of retail outlets
- Section 387n - Jurisdiction of and coordination with the Federal Trade Commission
- Section 387o - Regulation requirement
- Section 387p - Preservation of State and local authority
- Section 387q - Tobacco Products Scientific Advisory Committee
- Section 387r - Drug products used to treat tobacco dependence
- Section 387s - User fees
- Section 387t - Labeling, recordkeeping, records inspection
- Section 387u - Studies of progress and effectiveness
- Section 387v - Reporting on tobacco regulation activities