Label: VICHY LABORATOIRES NORMADERM SOS ACNE RESCUE SPOT CORRECTOR- sulfur lotion

  • NDC Code(s): 49967-648-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2023

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  • Active ingredient


    Sulfur 10%

  • Purpose

    Acne treatment

  • Use

    for the treatment of acne

  • Warnings

    For external use only

  • Do not use on

    • broken skin
    • large areas of the skin
  • When using this product

    • skin 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.
    • apply only to areas with acne
  • 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, niacinamide, zea mays (corn) starch, glycolic acid, stearyl alcohol, glycerin, octyldodecyl myristate, cetearyl alcohol, glyceryl stearate, sodium hydroxide, magnesium aluminum silicate, PEG-100 stearate, c13-14 isoparaffin, allantoin, ceteareth-20, phenoxyethanol, phenylethyl resorcinol, tocopheryl acetate, disodium EDTA, laureth-7, hydrogenated lecithin, polyacrylamide, ethylhexylglycerin

  • Questions or comments?

    1-877-378-4249

  • PRINCIPAL DISPLAY PANEL

    image of a carton

    image of a carton
  • INGREDIENTS AND APPEARANCE
    VICHY LABORATOIRES NORMADERM SOS ACNE RESCUE SPOT CORRECTOR 
    sulfur lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-648
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    OCTYLDODECYL MYRISTATE (UNII: S013N99GR8)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    ALLANTOIN (UNII: 344S277G0Z)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PHENYLETHYL RESORCINOL (UNII: G37UFG162O)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    LAURETH-7 (UNII: Z95S6G8201)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    NYLON-12 (UNII: 446U8J075B)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-648-011 in 1 CARTON12/01/2020
    120 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/01/2020
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    Englewood Lab, Inc.172198223manufacture(49967-648)
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