Label: GARNIER CLEAN BLACKHEAD ELIMINATING SCRUB- salicylic acid gel

  • NDC Code(s): 49967-035-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 2, 2024

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  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    for the treatment of acne

  • Warnings

    For external use only

  • 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.

  • Keep out of reach of children.

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

  • Directions

    - wet hands and face

    - squeeze scrub into hands and rub together

    - apply to face and massage gently, avoiding contact with eyes. If contact occurs, rinse eyes thoroughy with water.

    - rinse face thoroughly

  • Inactive ingredients

    water, sodium laureth sulfate, polyethylene, sodium chloride, acrylates copolymer, coco-betaine, cocamide MEA, glycerin, charcoal powder, citric acid, iron oxides, polyglycerin-10, polyglyceryl-10 myristate, polyglyceryl-10 stearate, PPG-5-ceteth-20, sodium hydroxide, trisodium ethylenediamine, disuccinate, fragrance

  • PRINCIPAL DISPLAY PANEL

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    image of a label
  • INGREDIENTS AND APPEARANCE
    GARNIER CLEAN BLACKHEAD ELIMINATING SCRUB 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-035
    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)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    POLYGLYCERIN-10 (UNII: P9060O936A)  
    POLYGLYCERYL-2 MYRISTATE (UNII: 0N6CWK1N09)  
    POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-035-01150 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00601/01/2014
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.624244349manufacture(49967-035)
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