Label: VICHY LABORATOIRES NORMADERM PHYTOACTION ACNE CONTROL DAILY MOISTURIZER- salicylic acid gel

  • NDC Code(s): 49967-606-01, 49967-606-02, 49967-606-03
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • Active ingredient

    Salicylic acid...2%

  • Purpose

    Acne treatment

  • Use

    for the treatment of acne

  • Warnings

    For external use only

  • When using this product

    kin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. if irritation occurs, only use one topical acne medication at a time.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • 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, isononyl isononanoate, butylene glycol, kaolin, zinc sulfate, bifida ferment lysate, sodium hydroxide, sodium polyacrylate, sodium hyaluronate, sodium benzoate, phenoxyethanol, ascorbyl glucoside, hydrolyzed algin, trisodium ethylenediamine disuccinate, biosaccharide gum-1, acrylates/c10-30 alkyl acrylate crosspolymer, fragrance

  • Questions or comments?

    Call toll free 1-877-378-4245

    Monday - Friday (9 a.m. to 5 p.m. EST)

  • PRINCIPAL DISPLAY PANEL

    image of a label

    image of a label
  • INGREDIENTS AND APPEARANCE
    VICHY LABORATOIRES NORMADERM PHYTOACTION ACNE CONTROL DAILY MOISTURIZER 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-606
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    KAOLIN (UNII: 24H4NWX5CO)  
    ZINC SULFATE (UNII: 89DS0H96TB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-606-011 in 1 CARTON09/01/2020
    150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49967-606-021 in 1 CARTON09/01/202006/01/2023
    23 mL in 1 TUBE; Type 0: Not a Combination Product
    3NDC:49967-606-031.5 mL in 1 PACKET; Type 0: Not a Combination Product09/01/202006/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/01/2020
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    COSMETIQUE ACTIVE PRODUCTION282658798manufacture(49967-606) , pack(49967-606)
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