Label: AMERICAN RED CROSS ANTISEPTIC CLEANSING- benzalkonium spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 25, 2024

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  • Active ingredient

    Benzalkonium Cl 0.13%

  • Uses

    First aid to help prevent the risk of bacterial contamination or skin infection associated with minor: cuts, scrapes, burns.

  • Warnings

    For external use only

    Do not use

    • in or near the eyes
    • over large sreas of the body or in large quantities
    • longer than 1 week
    • over raw surfaces or blistered areas.

    Ask a doctor before use if you have

    Ask a doctor before use if you have:

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    Stop use and ask a doctor if

    • condition or symptoms get worse or last more than 1 week
    • symptoms clear up and occurs again within a few days.

    Keep out of reach of children.

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

  • Directions

    Adults and children 2 years of age and older

    • clean the affected area
    • spray a small amount of this product on the area 1 to 3 times daily.
    • may be covered with a sterile bandage
    • if bandaged, let dry first
    • children under 2 years of age: consult a doctor
  • Purpose

    First aid antiseptic

  • Other information

    • protect from freezing or excessive heat
    • store at room temperature
  • Inactive ingredients

    Water(Aqua)

    1,2-Propanediol

    Lactic acid

  • label

    label

  • INGREDIENTS AND APPEARANCE
    AMERICAN RED CROSS ANTISEPTIC CLEANSING 
    benzalkonium spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51628-4440
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51628-4440-1177 mL in 1 BOTTLE; Type 0: Not a Combination Product12/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/24/2024
    Labeler - MY IMPORTS USA LLC (195767988)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Guoyao Jingyue Aerosol Co., Ltd.554529812manufacture(51628-4440)
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