Label: DR THROWERS OILY SKIN FACIAL ASTRINGENT- salicylic acid 2% liquid

  • NDC Code(s): 72839-611-02
  • Packager: Derma Care Research Labs, LLC
  • 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 27, 2022

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  • Active Ingredient

    Salicylic Acid 2%

  • Purpose

    Acne treatment.

  • Uses

    Dries and clears acne blemishes and allows skin to heal.

  • Warnings

    For external use only.

    Flammable--Keep away from open fire or flame.

    When using this product skin irritation and dryness are 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

    • Clean the skin thoroughly before applying this product
    • Using a cotton ball, cover the entire affected area with a thin layer one to three times daily
    • Avoid eye area, corner of the nose, and around the mouth area
    • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or directed by a doctor
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day

  • Inactive Ingredients

    Alcohol denat., benzoic acid, blue 1, boric acid, butylene glycol, eucalyptus globulus leaf oil, lavandula angustifolia (lavender) oil, mentha piperita (peppermint) oil, menthol, polysorbate 20, red 33, water.

  • Label

    Label

  • INGREDIENTS AND APPEARANCE
    DR THROWERS OILY SKIN FACIAL ASTRINGENT 
    salicylic acid 2% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72839-611
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    ALCOHOL (UNII: 3K9958V90M)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    MENTHOL (UNII: L7T10EIP3A)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72839-611-0257 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D09/28/2021
    Labeler - Derma Care Research Labs, LLC (116817470)
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