Label: PHISODERM CLEAN ANTI-BLEMISH FACIAL CLEANSER- salicylic acid gel
- NDC Code(s): 10742-1235-1
- 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
- Directions
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Inactive ingredients
water, lauramidopropyl betaine, sodium C14-16 olefin sulfonate, lauryl glucoside, aloe barbadensis leaf juice, aminomethyl propanol, butylene glycol, caprylyl/capryl glucoside, carica papaya (papaya) fruit extract, chamomilla recutita (matricaria) flower extract, disodium EDTA, fragrance, glycerin, hydroxyphenyl propamidobenzoic acid, hydroxypropyltrimonium hyaluronate, pentylene glycol, potassium sorbate, sodium benzoate, sodium chloride, tocopheryl acetate [vitamin E]
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INGREDIENTS AND APPEARANCE
PHISODERM CLEAN ANTI-BLEMISH FACIAL CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1235 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 GLYCERIN (UNII: PDC6A3C0OX) HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77) DIHYDROXYPROPYLTRIMONIUM (UNII: 925G44QFFO) PENTYLENE GLYCOL (UNII: 50C1307PZG) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) ALOE VERA LEAF (UNII: ZY81Z83H0X) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) PAPAYA (UNII: KU94FIY6JB) CHAMOMILE (UNII: FGL3685T2X) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1235-1 177 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 Drug M006 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(10742-1235)