Subchapter IX · MISCELLANEOUS
Contents (36)
- Section 387Definitions
- Section 387aFDA authority over tobacco products
- Section 387a-1Final rule
- Section 387bAdulterated tobacco products
- Section 387cMisbranded tobacco products
- Section 387dSubmission of health information to the Secretary
- Section 387eAnnual registration
- Section 387fGeneral provisions respecting control of tobacco products
- Section 387f-1Enforcement action plan for advertising and promotion restrictions
- Section 387gTobacco product standards
- Section 387hNotification and other remedies
- Section 387iRecords and reports on tobacco products
- Section 387jApplication for review of certain tobacco products
- Section 387kModified risk tobacco products
- Section 387lJudicial review
- Section 387mEqual treatment of retail outlets
- Section 387nJurisdiction of and coordination with the Federal Trade Commission
- Section 387oRegulation requirement
- Section 387pPreservation of State and local authority
- Section 387qTobacco Products Scientific Advisory Committee
- Section 387rDrug products used to treat tobacco dependence
- Section 387sUser fees
- Section 387tLabeling, recordkeeping, records inspection
- Section 387uStudies of progress and effectiveness
- Section 387vReporting on tobacco regulation activities
- Section 391Separability clause
- Section 392Exemption of meats and meat food products
- Section 393Food and Drug Administration
- Section 393aOffice of Pediatric Therapeutics
- Section 394Scientific review groups
- Section 395Loan repayment program
- Section 396Practice of medicine
- Section 397Contracts for expert review
- Section 398Notices to States regarding imported food
- Section 399Grants to States for inspections
- Section 399aOffice of the Chief Scientist