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
Drug Label Information
Updated December 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
- Directions
-
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
- Questions?
- Package/Label Principal Display Panel
-
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 Drug M006 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)