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United States Code (Last Updated: May 24, 2014) |
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Title 21. FOOD AND DRUGS |
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Chapter 9. FEDERAL FOOD, DRUG, AND COSMETIC ACT |
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SubChapter IX. TOBACCO PRODUCTS |
| § 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 |
Prior Provisions
A prior subchapter IX of this chapter, consisting of sections 391 to 399a of this title, was redesignated subchapter X by Pub. L. 111–31, div. A, title I, § 101(b)(1),