Label: PHISODERM CLEAR CONFIDENCE FACE SCRUB- salicylic acid gel
- NDC Code(s): 10742-1233-1
- 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
- Warnings
- Keep out of reach of children.
- Directions
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Inactive ingredients
acrylates copolymer, aloe barbadensis leaf juice, anhydrous citric acid, butylene glycol, cocamidopropyl betaine, diazolidinyl urea, edetate disodium, fragrance, glycerin, iron oxides, jojoba esters, methylparaben, microcrystalline wax, PEG-8/SMDI copolymer, portulaca oleracea extract, potassium C12-13 alkyl phosphate, propylene glycol, propylparaben, purified water, sodium C14-16 olefin sulfonate, trolamine, violet 2
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INGREDIENTS AND APPEARANCE
PHISODERM CLEAR CONFIDENCE FACE SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1233 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 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) D&C VIOLET NO. 2 (UNII: 350KA7O6HK) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) EDETATE DISODIUM (UNII: 7FLD91C86K) FERRIC OXIDE RED (UNII: 1K09F3G675) GLYCERIN (UNII: PDC6A3C0OX) HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N) METHYLPARABEN (UNII: A2I8C7HI9T) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6) PURSLANE (UNII: M6S840WXG5) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1233-1 142 g in 1 TUBE; Type 0: Not a Combination Product 05/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 05/01/2012 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-1233)