Label: PHISODERM ANTI BLEMISH BODY WASH- salicylic acid liquid
- NDC Code(s): 10742-8451-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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
- Directions
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Inactive ingredients
water, sodium laureth sulfate, disodium cocoamphodiacetate, cocamidopropyl betaine, sodium methyl cocoyl taurate, methyl gluceth-20, glycerin, aloe barbadensis leaf juice, anhydrous citric acid, butylene glycol, chamomilla recutita (matricaria) flower extract, diazolidinyl urea, disodium EDTA, fragrance, hydroxyphenyl propamidobenzoic acid, methylparaben, pentylene glycol, polysorbate 20, propylene glycol, propylparaben, tocopheryl acetate [vitamin E]
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INGREDIENTS AND APPEARANCE
PHISODERM ANTI BLEMISH BODY WASH
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-8451 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 LAURETH-3 SULFATE (UNII: BPV390UAP0) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) METHYL GLUCETH-20 (UNII: J3QD0LD11P) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 1,2-BUTANEDIOL (UNII: RUN0H01QEU) CHAMOMILE (UNII: FGL3685T2X) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) EDETATE DISODIUM (UNII: 7FLD91C86K) HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77) METHYLPARABEN (UNII: A2I8C7HI9T) PENTYLENE GLYCOL (UNII: 50C1307PZG) POLYSORBATE 20 (UNII: 7T1F30V5YH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-8451-1 295 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/01/2013 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-8451)