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
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 February 7, 2023
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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
- Questions?
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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 final part333D 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)