Label: BP WASH- benzoyl peroxide emulsion

  • NDC Code(s): 24470-901-05, 24470-901-08
  • Packager: CINTEX SERVICES, 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 December 22, 2020

If you are a consumer or patient please visit this version.

  • Active ingredient

    Benzoyl peroxide 10%

  • Purpose

    Acne treatment

  • Use

    For the treatment of acne

  • Warnings

    For external use only

    Do not use
    if you

    • have very sensitive skin
    • are sensitive to benzoyl peroxide


    When using this product

    • skin irritation and dryness is 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.
    • avoid unnecessary sun exposure and use a sunscreen
    • avoid contact with the eyes, lips, and mouth
    • avoid contact with hair and dyed fabrics, which may be bleached by this product
    • skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.


    Stop use and ask a doctor if irritation becomes severe.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.
    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • clean the skin thoroughly before applying this product
    • cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
    • 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 as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
    • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
  • Other information

    Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (between 59°F and 86°F).

  • Inactive ingredients

    carbomer, cetearyl alcohol, cocamidopropyl betaine, dimethyl isosorbide, hydrogenated castor oil, imidurea, methylparaben, mineral oil, PEG-14M, salicylic acid, sodium cocyl isethionate, sodium hydroxide, titanium dioxide, water, zea mays (corn) starch

  • Questions?

    1-855-899-4237

  • PRINCIPAL DISPLAY PANEL

    label1.jpg

    label2.jpg

  • INGREDIENTS AND APPEARANCE
    BP WASH 
    benzoyl peroxide emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24470-901
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    IMIDUREA (UNII: M629807ATL)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24470-901-05142 g in 1 BOTTLE; Type 0: Not a Combination Product01/15/2012
    2NDC:24470-901-08227 g in 1 BOTTLE; Type 0: Not a Combination Product01/15/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D01/15/2012
    Labeler - CINTEX SERVICES, LLC (078304114)