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Medi-first Burn First Aid (Unifirst First Aid Corporation)

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AEROSOL, SPRAY 85 g in 1 BOTTLE, SPRAY (47682-213-17) Label Information

Complete Medi-first Burn First Aid Information

  • Active Ingredients

    Benzethonium Chloride .2% w/w
    Benzocaine 10% w/w
    Menthol .33% w/w


  • Purpose

    Topical Antiseptic
    Topical Anesthetic
    Topical Anesthetic


  • Uses

    For temporary relief of pain, itching and to help protect against infection in

    minor cuts and scrapes
    minor skin irritations
    insect bites
    burns and sunburn 


  • 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 above 120° F 


  • Do not use

    in or near eyes or other mucus membranes
    in case of serious burns
    in case of deep or puncture wounds
    for prolonged period of time
    on a large portion of the body 


  • Stop use and ask a doctor if

    condition worsens or symptoms persist for more than 7 days
    condition clears up and recurs within a few days
    redness, swelling, or irritation occurs 


  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • Directions

    clean the affected area
    shake can well before using
    hold 4-6 inches from surface and spray area until wet
    may be covered with a sterile bandage. If bandaged, let dry first
    for adult institutional use only
    not intended for use on children 


  • Other information

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


  • Inactive Ingredients

    dipropylene glycol, isobutane, n-butane, propane


  • Questions or comments? ï»¿1-800-634-7680


  • Principal Display

    image description


  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST BURN FIRST AID 
    benzethonium chloride, benzocaine, and menthol aerosol, spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-213(NDC:52982-101)
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 8500 mg  in 85 g
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 170 mg  in 85 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 281 mg  in 85 g
    Inactive Ingredients
    Ingredient Name Strength
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    ISOBUTANE (UNII: BXR49TP611)  
    BUTANE (UNII: 6LV4FOR43R)  
    PROPANE (UNII: T75W9911L6)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-213-17 85 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 04/05/2013 05/01/2018
    Labeler - Unifirst First Aid Corporation (832947092)
    Registrant - Dixon Investments, Inc. (115315822)
    Establishment
    Name Address ID/FEI Business Operations
    Dixon Investments, Inc. 115315822 manufacture(47682-213)