FOOD AND DRUGS SUBCHAPTER IX-TOBACCO PRODUCTS

§§ 387–387f-1 · 25 sections

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails.

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§ 387Definitions § 387lJudicial review § 387oRegulation requirement § 387aFDA authority over tobacco products § 387bAdulterated tobacco products § 387cMisbranded tobacco products § 387dSubmission of health information to the Secretary § 387eAnnual registration § 387fGeneral provisions respecting control of tobacco products § 387gTobacco product standards § 387hNotification and other remedies § 387iRecords and reports on tobacco products § 387jApplication for review of certain tobacco products § 387kModified risk tobacco products § 387mEqual treatment of retail outlets § 387nJurisdiction of and coordination with the Federal Trade Commission § 387pPreservation of State and local authority § 387qTobacco Products Scientific Advisory Committee § 387rDrug products used to treat tobacco dependence § 387sUser fees § 387tLabeling, recordkeeping, records inspection § 387uStudies of progress and effectiveness § 387vReporting on tobacco regulation activities § 387a-1Final rule § 387f-1Enforcement action plan for advertising and promotion restrictions

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Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. Text of the U.S. Code 2024 Edition (govinfo), imported 2026-07-04. Amendments enacted after the 2024 Edition are not reflected. Read the official text ↗

Source: United States Code / CFR (uscode.house.gov, govinfo.gov) — U.S. federal law, public domain (17 U.S.C. § 105).

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