Title 21Subchapter

Subchapter Ix—Tobacco Products

Contents

  1. § 387. Definitions
  2. § 387a. FDA authority over tobacco products
  3. § 387a–1. Final rule
  4. § 387b. Adulterated tobacco products
  5. § 387c. Misbranded tobacco products
  6. § 387d. Submission of health information to the Secretary
  7. § 387e. Annual registration
  8. § 387f. General provisions respecting control of tobacco products
  9. § 387f–1. Enforcement action plan for advertising and promotion restrictions
  10. § 387g. Tobacco product standards
  11. § 387h. Notification and other remedies
  12. § 387i. Records and reports on tobacco products
  13. § 387j. Application for review of certain tobacco products
  14. § 387k. Modified risk tobacco products
  15. § 387l. Judicial review
  16. § 387m. Equal treatment of retail outlets
  17. § 387n. Jurisdiction of and coordination with the Federal Trade Commission
  18. § 387o. Regulation requirement
  19. § 387p. Preservation of State and local authority
  20. § 387q. Tobacco Products Scientific Advisory Committee
  21. § 387r. Drug products used to treat tobacco dependence
  22. § 387s. User fees
  23. § 387t. Labeling, recordkeeping, records inspection
  24. § 387u. Studies of progress and effectiveness
  25. § 387v. Reporting on tobacco regulation activities