Label: ANTIBACTERIAL MEDICATED TONER -2% SALICYLIC ACID- salicylic aclid spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 23, 2020

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  • WARNINGS

    Warnings: For External Use Only

  • ACTIVE INGREDIENT

    Salicylic Acid - 2%

  • PURPOSE

    Acne Treatment

  • Uses

    Treats acne and helps prevent new acne blemishes from forming

  • WHEN USING

    When using this product keep out of eyes. If contact occurs, flush thoroughly with water

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. if swallowed, seek medical help or contact a Poison Control Center

  • Directions:

    use 1 to 3 times daily on cleansed skin. mist the skin concentratikng on areas of acne breakout. do not rinse. allow to dry thoroughly. if bothersome dryness or peeling occurs, reduce application to once a day.

  • Inactive Ingredients:

    Water, SD Alcohol 40, Isoceteth-20, Ethoxydiglycol, Aloe Leaf Juice, Allantoin, Willow Bark Extract, Witch Hazel Extract, Sage Extract, Eucalyptus Oil, Pine Tree Oil, Butylene Glycol, Aminomethyl Propanol, Disodium EDTA, FD&C Yellow 5, FD&C Blue 1

  • PRINCIPAL DISPLAY PANEL

    Antibacterial Medicated Toner

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL MEDICATED TONER -2% SALICYLIC ACID 
    salicylic aclid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70367-011
    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
    WITCH HAZEL (UNII: 101I4J0U34)  
    PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
    SAGE OIL (UNII: U27K0H1H2O)  
    WATER (UNII: 059QF0KO0R)  
    WILLOW BARK (UNII: S883J9JDYX)  
    ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)  
    ISOCETETH-20 (UNII: O020065R7Z)  
    ETHOXYDIGLYCOL BEHENATE (UNII: N76ISC4ZZO)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70367-011-0122 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/26/2014
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D08/26/2014
    Labeler - Only Yourx, Inc. (089207519)
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