Label: FIRST AID- benzalkonium chloride, benzocaine spray

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 18, 2024

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  • Active Ingredients

    Benzalkonium Chloride 0.1%

    Benzocaine 5.0%

  • Purpose

    Topical Antiseptic

    Topical Anethetic

  • Uses

    First aid to help protect against skin infection and for the temporary relief of pain and itching in

    • minor cuts and scrapes
    • bites
    • skin irritation
  • Warnings

    For external use only.

    Flammable, keep away from heat or flame

  • DO NOT USE

    Do not use

    • in or near the eyes
    • over large portions of the body
    • in large quantities, particularly over raw surfaces or blistered areas
    • on deep or puncture wounds
    • on animal bites
    • on serious burns
    • longer than 7 days unless directed by a doctor
  • STOP USE

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days
    • symptoms clear up and occur again within a few days
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 1-800-222-1222

  • Directions

    • clean affected area and spray 1 to 3 times daily
    • may be covered with a sterile bandage

    Children under 2 years of age: ask a doctor

  • Inactive Ingredients

    Isopropyl Alcohol, Purified Water

  • PRINCIPAL DISPLAY PANEL

    2717FirstAidv20f.jpg

  • INGREDIENTS AND APPEARANCE
    FIRST AID 
    benzalkonium chloride, benzocaine spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0212
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.001 mg  in 1 mg
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE.05 mg  in 1 mg
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50332-0212-160 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/06/1996
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02/06/1996
    Labeler - HART Health (069560969)
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