Label: DG DEEP CLEANING ASTRINGENT SENSITIVE SKIN- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60742-002-01 - Packager: BELVEDERE INTERNATIONAL INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 7, 2012
If you are a consumer or patient please visit this version.
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- INDICATIONS & USAGE
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WARNINGS
FOR EXTERNAL USE ONLY, Flammable, keep awat from open fire or flame, Using other topical acne medication at the same time or immediately following the use fo this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Rinse right away with water if it gets in eyes.
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DOSAGE & ADMINISTRATION
- CLEANSE SKIN THOROUGHLY BEFORE APPLYING MEDICATION
- MOISTEN A COTTON BALL AND 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 APPLICATION DAILY. THEN GRADUALLY INCREASE TO 2 OR 3 TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCOR. IF BOTHERSOME DRYING OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.
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INGREDIENTS AND APPEARANCE
DG DEEP CLEANING ASTRINGENT SENSITIVE SKIN
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60742-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) ISOCETETH-20 (UNII: O020065R7Z) SODIUM CITRATE (UNII: 1Q73Q2JULR) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZOPHENONE (UNII: 701M4TTV9O) ALOE (UNII: V5VD430YW9) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60742-002-01 240 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333D 01/31/2013 Labeler - BELVEDERE INTERNATIONAL INC. (247836356) Registrant - BELVEDERE INTERNATIONAL INC. (247836356) Establishment Name Address ID/FEI Business Operations BELVEDERE INTERNATIONAL INC. 247836356 manufacture(60742-002)