Label: PHISODERM CLEAN ANTI-BLEMISH BODY WASH- salicylic acid gel
- NDC Code(s): 10742-1234-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated February 7, 2023
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
- Directions
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Inactive ingredients
water, sodium C14-16 olefin sulfonate, disodium cocoamphodiacetate, cocamidopropyl betaine, sodium methyl cocoyl taurate, glycerin, acrylates copolymer, aloe barbadensis leaf juice, butylene glycol, caprylyl/capryl glucoside, chamomilla recutita (matricaria) flower extract, citric acid, disodium EDTA, hydroxyphenyl propamidobenzoic acid, hydroxypropyltrimonium hyaluronate, melaleuca alternifolia (tea tree) leaf oil, pentylene glycol, potassium sorbate, sodium benzoate, sodium chloride, sodium hydroxide, tocopheryl acetate [vitamin E]
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INGREDIENTS AND APPEARANCE
PHISODERM CLEAN ANTI-BLEMISH BODY WASH
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1234 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 in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) GLYCERIN (UNII: PDC6A3C0OX) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) ALOE VERA LEAF (UNII: ZY81Z83H0X) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) CHAMOMILE (UNII: FGL3685T2X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77) DIHYDROXYPROPYLTRIMONIUM (UNII: 925G44QFFO) TEA TREE OIL (UNII: VIF565UC2G) PENTYLENE GLYCOL (UNII: 50C1307PZG) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1234-1 295 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/02/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 07/02/2021 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-1234)