Label: OXY DETOX CARE INVISIBLE HEALING TREATMENT PATCHES- salicylic acid patch
- NDC Code(s): 10742-1101-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
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Directions
- cleanse skin thoroughly before applying this product
- apply patch(es) to affected area(s)
- to remove, gently peel back patch and discard
- 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 doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Storage and Handling
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Inactive ingredients
acrylates/ethylhexyl acrylate copolymer, water, nonoxynol-30, alcohol denatured, butylene glycol, C13-14 isoparaffin, epilobium angustifolium flower/leaf/stem extract, kaolin, laureth-7, melaleuca alternifolia (tea tree) leaf oil, phenoxyethanol, phytosphingosine, polysorbate 80, PVP, sodium hyaluronate, sodium hydroxide, sodium metabisulfite, sodium polyacrylate, vitis vinifera (grape) seed extract, volcanic ash
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INGREDIENTS AND APPEARANCE
OXY DETOX CARE INVISIBLE HEALING TREATMENT PATCHES
salicylic acid patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1101 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 Inactive Ingredients Ingredient Name Strength 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG) WATER (UNII: 059QF0KO0R) NONOXYNOL-30 (UNII: JJX07DG188) ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) EPILOBIUM ANGUSTIFOLIUM WHOLE (UNII: C278QS9YBT) KAOLIN (UNII: 24H4NWX5CO) LAURETH-7 (UNII: Z95S6G8201) TEA TREE OIL (UNII: VIF565UC2G) PHENOXYETHANOL (UNII: HIE492ZZ3T) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM METABISULFITE (UNII: 4VON5FNS3C) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) VITIS VINIFERA SEED (UNII: C34U15ICXA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1101-1 30 in 1 CARTON; Type 0: Not a Combination Product 06/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/15/2022 Labeler - The Mentholatum Company (002105757)