• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

CFR - Code of Federal Regulations Title 21

  • Print
  • Share
  • E-mail
-

The information on this page is current as of Dec 22, 2023.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

New Search
Help | More About 21CFR
TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER D - DRUGS FOR HUMAN USE
 
PART 355ANTICARIES DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
 

Subpart A - General Provisions
   § 355.1 - Scope.
   § 355.3 - Definitions.

Subpart B - Active Ingredients
   § 355.10 - Anticaries active ingredients.
   § 355.20 - Packaging conditions.

Subpart C - Labeling
   § 355.50 - Labeling of anticaries drug products.
   § 355.55 - Principal display panel of all fluoride rinse drug products.
   § 355.60 - Professional labeling.

Subpart D - Testing Procedures
   § 355.70 - Testing procedures for fluoride dentifrice drug products.

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

-
-