Label: ALMAY CLEAR COMPLEXION PRESSED POWDER- salicylic acid powder
- NDC Code(s): 0311-0721-80
- Packager: Almay, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 22, 2019
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Uses:
- Warnings:
-
Directions
Clean skin thoroughly
before applying this product • Cover the
entire affected area with a thin layer 1 to 3
times daily. • Because excessive drying of
the skin may occur, start with 1 appli -
cation daily, then gradually increase to 2
or 3 times daily if needed or as directed
by doctor. • If bothersome dryness or
peeling occurs, reduce application to once
a day or every other day. - Inactive Ingredients
- DOSAGE & ADMINISTRATION
- Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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INGREDIENTS AND APPEARANCE
ALMAY CLEAR COMPLEXION PRESSED POWDER
salicylic acid powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0311-0721 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.002 g in 1 g Inactive Ingredients Ingredient Name Strength MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) WATER (UNII: 059QF0KO0R) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) PHENOXYETHANOL (UNII: HIE492ZZ3T) TALC (UNII: 7SEV7J4R1U) MAGNESIUM STEARATE (UNII: 70097M6I30) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) NYLON-12 (UNII: 446U8J075B) KAOLIN (UNII: 24H4NWX5CO) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0311-0721-80 8 g in 1 CONTAINER; Type 0: Not a Combination Product 01/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 01/02/2019 Labeler - Almay, Inc. (064988652) Establishment Name Address ID/FEI Business Operations REVLON, INC. 809725570 manufacture(0311-0721)