Label: CVS PHARMACY CLEAR SKIN DAILY MOISTURIZER- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-152-04 - Packager: CVS PHARMACY
- 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 December 1, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- USES
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WARNINGS
FOR EXTERNA USE ONLY
WHEN USING THIS PRODUCT
- USING OTHER TOPICAL ACNE MDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.
- AVOID CONTACT WITH EYES. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER
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DIRECTIONS
- CLEANSE THE SKIN THOROUGHLY BEFORE APPLYING MEDICATION
- COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER ONE TO THREE TIMES DAILY
- BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH ONE APPLICATION DAILY, THEN GRADUALLY INCREASE TO TWO TO THREE TIMES DAILY, IF NEEDED, OR AS DIRECTED BY A DOCTOR. IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APLICATION TO ONCE A DAY OR EVERY OTHER DAY
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INACTIVE INGREDIENTS
ARACHIDYL ALCOHOL, ARACHIDYL GLUCOSIDE, BEHENYL ALCOHOL, BHT, BIS-PHENYLPROPYL DIMETHICONE, C12-15 ALKYL BENZOATE, C13-14 ISOPARAFFIN, CETEARYL ALCOHOL, CETEARYL GLUCOSIDE, CITRIC ACID, DIMETHICONE, DISODIUM EDTA, ETHYLENE/ACRYLIC ACID COPOLYMER, ETHYLHEXYLGLYCERIN, FRAGRANCE (PARFUM), GLYCERIN, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, ISOCETETH-20, LAURETH-7, METHYL GLUCETH-20, PHENOXYETHANOL, PPG-15 STEARYL ETHER, SODIUM HYDROXIDE, WATER (AQUA)
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- LABEL COPY
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INGREDIENTS AND APPEARANCE
CVS PHARMACY CLEAR SKIN DAILY MOISTURIZER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-152 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) DOCOSANOL (UNII: 9G1OE216XY) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) SOYBEAN (UNII: L7HT8F1ZOD) ISOCETETH-20 (UNII: O020065R7Z) LAURETH-7 (UNII: Z95S6G8201) METHYL GLUCETH-20 (UNII: J3QD0LD11P) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-152-04 118 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/30/2014 Labeler - CVS PHARMACY (062312574) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(59779-152)
