Label: CLARIFYING PEEL- salicylic acid gel

  • NDC Code(s): 46007-102-11, 46007-102-12
  • Packager: Skin Authority LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 5, 2023

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  • ACTIVE INGREDIENT

    SALICYLIC ACID 2%

  • PURPOSE

    ACNE TREATMENT

  • USES

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

  • WARNINGS

    FOR EXTERNAL USE ONLY.

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

    IF IRRITATION DEVELOPS, DISCONTINUE USE.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • 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.

  • OTHER INGREDIENTS

    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?

    +1-760-268-0047

  • PRINCIPAL DISPLAY PANEL

    0-Image_Clarifying Liquid01b LBL (DF Box)_Clarifying Liquid

  • INGREDIENTS AND APPEARANCE
    CLARIFYING PEEL 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46007-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:46007-102-1250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/19/2012
    2NDC:46007-102-1120 mL in 1 TUBE; Type 0: Not a Combination Product04/19/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00604/19/2012
    Labeler - Skin Authority LLC (136549396)
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