Label: VICHY LABORATOIRES NORMADERM ACNE CONTROL MOISTURIZER- salicylic acid gel
- NDC Code(s): 69625-661-01
- Packager: COSMETIQUE ACTIVE PRODUCTION
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 11, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Flammable until dry.
- 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 increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day -
Inactive ingredients
water, glycerin, butylene glycol, isononyl isononanoate, kaolin, hydrolyzed algin, zinc sulfate, bifida ferment lysate, sarcosine, sodium hyaluronate, sodium hydroxide, trisodium ethylenediamine disuccinate, ascorbyl glucoside, acetic acid, acrylates/c10-30 alkyl acrylate crosspolymer, biosaccharide gum-1, caprylyl glycol, lactic acid, maltodextrin, pentylene glycol, sodium polyacrylate, xanthan gum, sodium benzoate, fragrance
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INGREDIENTS AND APPEARANCE
VICHY LABORATOIRES NORMADERM ACNE CONTROL MOISTURIZER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69625-661 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) GLYCERIN (UNII: PDC6A3C0OX) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) KAOLIN (UNII: 24H4NWX5CO) ZINC SULFATE (UNII: 89DS0H96TB) SARCOSINE (UNII: Z711V88R5F) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM HYDROXIDE (UNII: 55X04QC32I) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) ACETIC ACID (UNII: Q40Q9N063P) BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H) CAPRYLYL GLYCOL (UNII: 00YIU5438U) LACTIC ACID (UNII: 33X04XA5AT) MALTODEXTRIN (UNII: 7CVR7L4A2D) PENTYLENE GLYCOL (UNII: 50C1307PZG) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69625-661-01 1 in 1 CARTON 06/01/2023 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2023 Labeler - COSMETIQUE ACTIVE PRODUCTION (282658798) Establishment Name Address ID/FEI Business Operations COSMETIQUE ACTIVE PRODUCTION 282658798 manufacture(69625-661) , pack(69625-661)