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ELF Zit Zapping Conceler (J. A. Cosmetics U.S. INC)

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PASTE 1.5 g in 1 TUBE (76354-018-01) Label Information

Complete ELF Zit Zapping Conceler Information

  • ACTIVE INGREDIENT

    Active Ingredient:

    Salicylic Acid 1.0%


  • PURPOSE

    PURPOSE

    ACNE TREATMENT


  • INDICATIONS & USAGE

    Uses

    • For the treatment of acne
    • Helps prevent new acne blemishes

  • WARNINGS

    Warning:

    For external use only


  • WHEN USING

    When Using This Product

    • Keep out of eyes, rinse with water to remove.
    • Using other tropical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin.  If this occurs, only one medication should be used unless directed by a doctor.

  • ASK DOCTOR

    Stop use and ask a doctor if

    • rash occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep Out of Reach of Children


  • DOSAGE & ADMINISTRATION

    Directions:

    • Cleanse the skin thoroughly before applying medication. Cover the entire affected area with a thin layer one to three times daily. Because excessive drying of 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.

  • STORAGE AND HANDLING

    Other Information:

    Protect the product in its container from excessive heat and direct sun.


  • INACTIVE INGREDIENT

    Inactive Ingredient:

    Caprylic/Capric Triglyceride, Ethylhexyl Palmitate, Octyldodecanol, Diisostearyl Malate, Methyl Methacrylate Crosspolymer, Mica, Polyglyceryl-4 Isostearate, Microcrystalline Wax (Cera Microcristallina), Camphor, Melaleuca Alternafolia (Tea Tree) Leaf Oil

    May Contain:

    Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499), Blue 1 Lake (CI 42090)


  • INGREDIENTS AND APPEARANCE
    ELF ZIT ZAPPING CONCELER 
    salicylic acid paste
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-018
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.0 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)  
    METHYL METHACRYLATE (UNII: 196OC77688)  
    MICA (UNII: V8A1AW0880)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:76354-018-51 1 in 1 PACKAGE
    1 NDC:76354-018-01 1.5 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 01/02/2012
    Labeler - J. A. Cosmetics U.S. INC (186705047)
    Registrant - J. A. Cosmetics U.S. INC (186705047)