Label: MEDI-FIRST ANTISEPTIC WIPES- benzalkonium chloride swab
MEDI-FIRST PLUS ANTISEPTIC WIPES- benzalkonium chloride swab

  • NDC Code(s): 47682-030-71, 47682-212-12, 47682-212-33, 47682-212-71
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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  • Drug Facts

    Active ingredient
    Benzalkonium chloride 0.133% w/v

  • Purpose

    First aid antiseptic

  • Uses

    First aid to help prevent infection in minor cuts, scrapes, and burns.

  • Warnings

    Do not use

    • in the eyes or over large areas of the body
    • in case of deep or puncture woulds, animal bite or serious burns, consult a doctor
    • longer than 1 week unless directed by a doctor

    Stop use and ask a doctor if

    • if the 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

    • tear open packet, unfold and clean the affected area
    • discard after use
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • Other information

    • store at room temperature 59-86ºF (15-30ºC)
    • tamper evident sealed packets
    • do not use any open or torn packets
  • Inactive ingredients

    sodium bicarbonate, water

  • Questions or comments?

    1-800-634-7680

  • Medi-First Antiseptic Wipes Label

    Medi-First®

    Antiseptic Wipes

    Benzalkonium chloride 0.133%

    First aid Antiseptic

    Product # 21412

    Extra Large Wipes

    Net Contents: 10 units per box

    Medi Antiseptic

  • Medi-First Plus Antiseptic Wipes Label

    Medi First ®

    Plus

    Antiseptic Wipes

    Extra Large

    Benzalkonium chloride 0.133% w/v

    First Aid Antiseptic

    Reorder # 103071

    20 Wipes

    MFP Aniseptic

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST ANTISEPTIC WIPES 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-212
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.33 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-212-1210 in 1 BOX08/21/2017
    11.4 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-212-7120 in 1 BOX08/21/2017
    21.4 mL in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-212-33100 in 1 BOX08/21/2017
    31.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/21/2017
    MEDI-FIRST PLUS ANTISEPTIC WIPES 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-030-7120 in 1 BOX08/21/2017
    11.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/21/2017
    Labeler - Unifirst First Aid Corporation (832947092)
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