21 CFR Part 1100 - TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY

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Authority:
21 U.S.C. 387a(b), 387f(d); Secs. 901(b) and 906(d), Pub. L. 111-31; 21 CFR 16.1 and 1107.1; 21 CFR 1.1, 1.20, 14.55, 17.1, and 17.2. Section 1100.5 is issued under 21 U.S.C. 321, 353(g), and 371(a); 21 CFR 1.1.
Source:
81 FR 29102, May 10, 2016, unless otherwise noted.
{'United States Code': [{'Title': '21', 'Section': '321', 'headtext': ' Definitions; generally', 'cleanpath': '/uscode/text/21/321'}, {'Title': '21', 'Section': '353', 'headtext': ' Exemptions and consideration for certain drugs, devices, and biological products', 'cleanpath': '/uscode/text/21/353'}, {'Title': '21', 'Section': '371', 'headtext': ' Regulations and hearings', 'cleanpath': '/uscode/text/21/371'}, {'Title': '21', 'Section': '387a', 'headtext': ' FDA authority over tobacco products', 'cleanpath': '/uscode/text/21/387a'}, {'Title': '21', 'Section': '387f', 'headtext': ' General provisions respecting control of tobacco products', 'cleanpath': '/uscode/text/21/387f'}], 'Statutes at Large': [], 'Public Laws': [{'Congress': '111', 'Law Number': '111-31', 'headtext': 'Pub L. 111-31', 'cleanpath': 'https://www.law.cornell.edu/rio/citation/Pub._L._111-111-31'}], 'Presidential Documents': []}