• § 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