Title 21

PART 1100

Part 1100 - Tobacco Products Subject To Fda Authority

PART 1100 - TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY 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.

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.

21:8.0.1.4.47.0.1.1	SECTION 1100.1	1100.1 Scope.
21:8.0.1.4.47.0.1.2	SECTION 1100.2	1100.2 Requirements.
21:8.0.1.4.47.0.1.3	SECTION 1100.3	1100.3 Definitions.
21:8.0.1.4.47.0.1.4	SECTION 1100.5	1100.5 Exclusion from tobacco regulation.