Label: MEDI-FIRST ANTISEPTIC- benzalkonium chloride spray
ANTISEPTIC- benzalkonium chloride liquid

  • NDC Code(s): 47682-245-02, 47682-254-02
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    First aid antiseptic

  • Uses

    First aid to help prevent infection & for the temporary pain relief in minor cuts, scrapes and burns

  • WARNINGS

    Warnings

    For external use only.

    Flammable keep away from tire or flame

    Do not use

    • near eyes or mucous membranes
    • on deep or puncture wounds, animal bites, or serious burns
    • over large areas of the body
    • more than one week unless directed by a doctor

    Stop use and ask a doctor if

    condition persists or gets worse

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

  • Directions

    • clean affected area & spray 1 to 3 times daily
    • may be covered with a sterile bandage
    • not to be used on children under 12 years of age
  • Inactive ingredients

    ethyl alcohol, purified water

  • Questions or comments?

    1 -800-634-7680

  • Medi-First Antiseptic Spray Label

    MEDI-FIRST ®

    Antiseptic Spray

    Pump Spray

    Benzalkonium Chloride 0.13%

    First Aid Antiseptic

    • Treats minor cuts, scrapes and abrasion
    • Helps prevent infection

    2 FL OZ (59.1 ML)

    MF Antiseptic

  • Medi-First Antiseptic Spray Label

    Medi-First®

    Antiseptic Spray

    Pump Spray

    Benzalkonium Chloride 0.13%

    First Aid Antiseptic

    Treats minor cuts, scrapes and abrasions

    Helps prevent infection

    Store at 68°C-77°F (20°-25°C)

    2 FL OZ (59.1ML)

    Medi-First

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST ANTISEPTIC 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-254
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-254-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/01/2021
    ANTISEPTIC 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-245
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-245-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/10/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/10/2016
    Labeler - Unifirst First Aid Corporation (832947092)
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