21 C.F.R. PART 352--SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]
TITLE 21--Food and Drugs
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER D--DRUGS FOR HUMAN USE
PART 352--SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]
Subpart A--GENERAL PROVISIONS
Subpart B--ACTIVE INGREDIENTS
|
|
| Sunscreen active ingredients.
|
|
|
|
| Permitted combinations of active ingredients.
|
|
Subpart C--LABELING
|
|
| Principal display panel of all sunscreen drug products.
|
|
|
|
| Labeling of sunscreen drug products.
|
|
|
|
| Labeling of permitted combinations of active ingredients.
|
|
Subpart D--TESTING PROCEDURES
|
|
| Light source (solar simulator).
|
|
|
|
| General testing procedures.
|
|
|
|
| Determination of SPF value.
|
|
|
|
| Determination if a product is water resistant or very water resistant.
|
|
