Label: CLARIFYING TONER- salicylic acid liquid
- NDC Code(s): 62742-4240-1, 62742-4240-2
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 8, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive Ingredient:
Water (Aqua), Alcohol Denat, Hamamelis Virginiana (Witch Hazel) Leaf Water, Ethoxydiglycol, Niacinamide, Glycerin, Polysorbate 20, Plantago Ovata (Indian Plantin) Seed Extract, Sodium PCA, Hydrolyzed Wheat Protein, Hydrolyzed Wheat Starch, Phenoxyethanol, Caprylyl Glycol, Ethylhexyl Glycerin, Rosmarinus Officinalis ( Rosemary) Leaf Extract, Chamomilla Recutita ( Chamomile) Flower Extract, Hexylene Glycol, Allantoin, Dipotassium Glycyrrhizate.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLARIFYING TONER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4240 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 100 g Inactive Ingredients Ingredient Name Strength ROSEMARY (UNII: IJ67X351P9) MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02) ALLANTOIN (UNII: 344S277G0Z) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PLANTAGO OVATA SEED (UNII: UD50RBY30F) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) STARCH, WHEAT (UNII: 79QS2MG2LP) HEXYLENE GLYCOL (UNII: KEH0A3F75J) HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) WATER (UNII: 059QF0KO0R) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) NIACINAMIDE (UNII: 25X51I8RD4) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4240-1 120 g in 1 BOTTLE; Type 0: Not a Combination Product 12/08/2023 2 NDC:62742-4240-2 60 g in 1 BOTTLE; Type 0: Not a Combination Product 12/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 12/08/2023 Labeler - Allure Labs (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4240)