Label: OXY 3 IN 1 ACNE PADS- salicylic acid swab
- NDC Code(s): 10742-4359-1, 10742-4359-3
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
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 a pad to cleanse and cover the affected area with a thin layer of medicine 1 to 3 times daily
- because too much drying of the skin may occur, start with 1 application, 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
- Sensitivity test: Apply product sparingly to a small affected area for the first 3 days. If no discomfort occurs, follow directions above.
Other information
- KEEP TIGHTLY CLOSED
- avoid storing at temperatures above 100˚F (38˚C)
- protect from freezing
- keep away from flame, fire and heat
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
OXY 3 IN 1 ACNE PADS
salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-4359 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 ALCOHOL (UNII: 3K9958V90M) ALLANTOIN (UNII: 344S277G0Z) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) ISOCETETH-20 (UNII: O020065R7Z) ETHYL JOJOBATE (UNII: 2351QH8W1N) PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6) FYTIC ACID (UNII: 7IGF0S7R8I) WATER (UNII: 059QF0KO0R) EDETATE TRISODIUM (UNII: 420IP921MB) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-4359-1 90 in 1 JAR; Type 0: Not a Combination Product 08/01/2018 2 NDC:10742-4359-3 115 in 1 JAR; Type 0: Not a Combination Product 08/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/01/2018 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-4359)