Title 21

PART 355

Part 355 - Anticaries Drug Products For Over-the-counter Human Use

PART 355 - ANTICARIES DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Authority:21 U.S.C. 321, 351, 352, 353, 355, 360, 371. Source:60 FR 52507, Oct. 6, 1995, unless otherwise noted. Editorial Note:Nomenclature changes to part 355 appear at 69 FR 13717, Mar. 24, 2004.

• Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
• Source: 60 FR 52507, Oct. 6, 1995, unless otherwise noted.

21:5.0.1.1.28.1	SUBPART A	Subpart A - General Provisions
21:5.0.1.1.28.1.1.1	SECTION 355.1	355.1 Scope.
21:5.0.1.1.28.1.1.2	SECTION 355.3	355.3 Definitions.
21:5.0.1.1.28.2	SUBPART B	Subpart B - Active Ingredients
21:5.0.1.1.28.2.1.1	SECTION 355.10	355.10 Anticaries active ingredients.
21:5.0.1.1.28.2.1.2	SECTION 355.20	355.20 Packaging conditions.
21:5.0.1.1.28.3	SUBPART C	Subpart C - Labeling
21:5.0.1.1.28.3.1.1	SECTION 355.50	355.50 Labeling of anticaries drug products.
21:5.0.1.1.28.3.1.2	SECTION 355.55	355.55 Principal display panel of all fluoride rinse drug products.
21:5.0.1.1.28.3.1.3	SECTION 355.60	355.60 Professional labeling.
21:5.0.1.1.28.4	SUBPART D	Subpart D - Testing Procedures
21:5.0.1.1.28.4.1.1	SECTION 355.70	355.70 Testing procedures for fluoride dentifrice drug products.

---