Label: KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS TRULY TARGETED ACNE CLEARING SOLUTION- salicylic acid liquid
- NDC Code(s): 49967-055-01, 49967-055-02, 49967-055-03
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually ingrease to two or three times dialy if neded or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS TRULY TARGETED ACNE CLEARING SOLUTION
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-055 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) GLUCONOLACTONE (UNII: WQ29KQ9POT) NIACINAMIDE (UNII: 25X51I8RD4) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCOLIC ACID (UNII: 0WT12SX38S) SODIUM HYDROXIDE (UNII: 55X04QC32I) GLYCERIN (UNII: PDC6A3C0OX) METHYL GLUCETH-20 (UNII: J3QD0LD11P) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-055-01 1 in 1 CARTON 06/01/2023 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:49967-055-02 4 mL in 1 VIAL; Type 0: Not a Combination Product 06/01/2023 3 NDC:49967-055-03 2 mL in 1 PACKET; Type 0: Not a Combination Product 06/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2023 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-055) , pack(49967-055)