Label: OXY ADVANCED CARE MAXIMUM STRENGTH 3-IN-1 ACNE PADS- salicylic acid swab
- NDC Code(s): 10742-1200-1, 10742-1200-2
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- keep away from eyes, lips and mouth. If contact occurs, flush thoroughly with water.
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- do not leave pad on skin
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Directions
- use wipe to clean skin thoroughly
- 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 2 or 3 times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
OXY ADVANCED CARE MAXIMUM STRENGTH 3-IN-1 ACNE PADS
salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6) ISOCETETH-20 (UNII: O020065R7Z) ALLANTOIN (UNII: 344S277G0Z) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2) FYTIC ACID (UNII: 7IGF0S7R8I) TROLAMINE (UNII: 9O3K93S3TK) EDETATE TRISODIUM (UNII: 420IP921MB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1200-1 90 in 1 JAR; Type 0: Not a Combination Product 10/01/2021 2 NDC:10742-1200-2 104 in 1 JAR; Type 0: Not a Combination Product 10/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 10/01/2021 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-1200)