Label: RUGBY BENZOYL PEROXIDE WASH ACNE MEDICATION- benzoyl peroxide lotion

  • NDC Code(s): 75376-474-42
  • Packager: Guangzhou Danting Bath&Body Care Industry Co. Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 9, 2026

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzoyl peroxide USP 10%

    Purpose

    Acne medication

  • Use

    for the treatment of acne

  • Warnings

    For external use only

    Do not use this medication 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 consult a doctor if

    irritation becomes severe

    If pregnant or breastfeeding

    ask a health professional before use.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center
    (1-800-222-1222) 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

    • Keep tightly closed
    • Store at room temperature
  • Inactive ingredients

    Carbomer, Cetearyl Alcohol, Citric Acid, Disodium
    EDTA, Disodium Laureth Sulfosuccinate, Glyceryl Stearate, Magnesium
    Aluminum Silicate, Peg-100 Stearate, Propylene Glycol, Sodium Benzoate,
    Sodium C14-16 Olefin Sulfonate, Sodium Lauroamphoacetate, Xanthan
    Gum, Water

  • Questions or comments?

    1-866-306-9136

    You may also report serious side effects to this phone
    number
    Mon-Fri, 9:00 AM - 5:00 PM Eastern Time.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    RUGBY BENZOYL PEROXIDE WASH  ACNE MEDICATION
    benzoyl peroxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75376-474
    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
    CARBOMER (UNII: 0A5MM307FC)  
    CETEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75376-474-42237 g in 1 BOTTLE; Type 0: Not a Combination Product10/31/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00610/31/2025
    Labeler - Guangzhou Danting Bath&Body Care Industry Co. Ltd (545337886)
    Registrant - Medical Group Care LLC (085137089)
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