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ACNE AND OIL CONTROL (Skin Authority LLC)

Available Formats

Dosage Form Package Information Links
GEL 50 mL in 1 BOTTLE (46007-101-12) Label Information
GEL 20 mL in 1 TUBE (46007-101-11) Label Information

Complete ACNE AND OIL CONTROL Information

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:

    SALICYLIC ACID 2%


  • PURPOSE

    PURPOSE:

    ACNE TREATMENT


  • INDICATIONS & USAGE

    USES:

    HELPS ELIMINATE ACNE-CAUSING BACTERIA, CALMS INFLAMMATION, AND MINIMIZES EXCESS OIL.


  • WARNINGS

    WARNINGS:

    FOR EXTERNAL USE ONLY.


  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.


  • OTHER SAFETY INFORMATION

    AVOID CONTACT WITH  EYES AND EYELIDS. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.


  • STOP USE

    IF IRRITATION DEVELOPS, DISCONTINUE USE.


  • DOSAGE & ADMINISTRATION

    DIRECTIONS:

    APPLY WITH FINGERTIPS  OR COTTON PAD IMMEDIATELY AFTER CLEANSING, COVERING FACE AND INFLAMED AREAS. CONTINUE WITH DAILY CARE ROUTINE. REAPPLY THROUGHOUT THE DAY TO REMOVE EXCESS OIL AND DIRT.


  • INACTIVE INGREDIENT

    WATER, GLYCOLIC ACID, HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT, SD ALCOHOL, SODIUM PCA, PPG-5-CETETH-20, SODIUM HYDROXIDE, ALOE BARBADENSIS LEAF JUICE, POLYSORBATE 80, PHENOXYETHANOL, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, HEXYLENE GLYCOL, METHYLGLUCETH-20.


  • QUESTIONS

    QUESTIONS? +1-760-268-0047


  • PRINCIPAL DISPLAY PANEL

    SKIN AUTHORITY

    ACNE AND OIL CONTROL

    1.7 FL OZ / 50 ML

    51101(revE)50ml-AcneOilControl


  • INGREDIENTS AND APPEARANCE
    ACNE AND OIL CONTROL 
    salicylic acid gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:46007-101
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:46007-101-12 50 mL in 1 BOTTLE
    2 NDC:46007-101-11 20 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 04/19/2012
    Labeler - Skin Authority LLC (136549396)
    Registrant - Skin Authority LLC (136549396)