Label: FOAMING CLEANSER- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4168-1 - Packager: Allure Labs Inc
- 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 November 9, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- WHEN USING
- INDICATIONS & USAGE
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INACTIVE INGREDIENT
Water (Aqua), Alkyl (C10-16) Ether Sulfate Sodium Salt, Cocamidopropyl Betaine, Butylene Glycol, Hydrolyzed Wheat Protein, Alcohols (C12-15 Ln. saturated) Ethoxylate, Hydrolyzed Wheat Starch, Caprylyl Glycol, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hydroxide, Ethylhexyl Glycerin, Hexylene Glycol Sodium Chloride, Lavandula Angustifolia (Lavender) Leaf Oil O.E., Glycerin.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FOAMING CLEANSER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4168 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) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) C12-15 ALCOHOLS (UNII: 2C8M6XLB5C) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) ROSEMARY (UNII: IJ67X351P9) SODIUM HYDROXIDE (UNII: 55X04QC32I) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM CHLORIDE (UNII: 451W47IQ8X) LAVENDER OIL (UNII: ZBP1YXW0H8) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4168-1 125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/09/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/09/2018 Labeler - Allure Labs Inc (926831603)