Label: BANDAGE- benzocaine and benzethonium chloride aerosol, spray

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

Drug Label Information

Updated January 24, 2024

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  • Active Ingredients

    Benzocaine 10% w/w
    Benzethonium Chloride 0.2% w/w 

  • Purpose

    Topical Anesthetic
    Topical Antiseptic 

  • Uses

    First aid to help protect against infection in

    • minor cuts
    • scrapes
    • burns
  • Warnings

    For External Use Only

    Flammable

    • keep away from fire or flame
    • contents under pressure
    • do not puncture or incinerate container
    • do not expose to temperatures agove 120°F
  • Do not use

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

  • Stop use and ask doctor if

    • redness, swelling, or irritation occurs
    • infection occurs
    • condition persists or worsens
    • symptoms persist for more than 7 days 
  • Keep out of reach of children

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

  • Directions

    Adults and children 12 years of age and over:

    • clean the affected area
    • shake can well before using
    • hold 4 to 6 inches from surface and spray until area is covered with film
    • when dry, may be covered with a sterile bandage

    Children under 12 years of age: ask a doctor

  • Other information

    • avoid inhaling
    • use only as directed
    • intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal
  • Inactive Ingredients

    copovidone K35-31, ethyl alcohol, isobutane, n-butane,  propane

  • Principal Display

    2765spraybandagev21f.jpg2765spraybandagev21f.jpg

  • INGREDIENTS AND APPEARANCE
    BANDAGE 
    benzocaine and benzethonium chloride aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0218
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE170 mg  in 85 g
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE2720 mg  in 85 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    COPOVIDONE K25-31 (UNII: D9C330MD8B)  
    BUTANE (UNII: 6LV4FOR43R)  
    PROPANE (UNII: T75W9911L6)  
    ISOBUTANE (UNII: BXR49TP611)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50332-0218-185 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/01/1974
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM04/01/1974
    Labeler - HART Health (069560969)
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