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

  • NDC Code(s): 72839-613-02
  • 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 31, 2022

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  • Active Ingredient

    Salicylic Acid 2%

  • Purpose

    Acne treatment.

  • Uses

    For the treatment of acne.

  • Warnings

    For external use only.

    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.

    Stop use if dryness, redness, or itching occurs and see a physician if symptoms persist.

  • Keep Out of Reach of Children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Use morning and evening. Apply to wet skin with fingers, massage lightly to foam. Avoid eye area, corners of the nose are, and around the mouth. Rinse thoroughly with warm water. If bothersome dryness or peeling occurs, reduce application to once a day or every other day or discontinue the product.

  • Inactive Ingredients

    Ammonium laureth sulfate, ammonium lauryl sulfate, camphor, cocamide MEA, cocamidopropyl betaine, diazolidinyl urea, eucalyptus globulus leaf oil, glycol stearate, mentha piperita (peppermint) oil, menthol, methylparaben, PEG-150 pentaerythrityl tetrastearate, PEG-6 caprylic/capric glycerides, propylene glycol, propylparaben, sodium hydroxide, sodium laureth sulfate, water.

  • Label

    Label

  • INGREDIENTS AND APPEARANCE
    DR THROWERS OILY SKIN FACIAL CLEANSER 
    salicylic acid 2% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72839-613
    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
    PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
    MENTHOL (UNII: L7T10EIP3A)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72839-613-0257 g in 1 TUBE; 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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