Label: MEDICAINE STING AND BITE- benzocaine swab

  • NDC Code(s): 67777-405-01, 67777-405-02, 67777-405-03
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 24, 2024

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  • Active Ingredient

    Benzocaine USP 20%

  • Purpose

    Analgesic

  • Active Ingredient

    L-Menthol USP 1%

  • Purpose

    Analgesic

  • Use(s)

    For the temporary relief of pain and itching associated with insect bites and stings.

  • Warnings

    For External Use Only

    When Using Section

    • Do not use in the eyes

    • Not for prolonged use

    • Do not apply other medication to the same affected areas unless advised by a doctor

    Stop use and ask a doctor if

    Condition persists, or if a rash, irritation, or allergic reaction develops.

    Keep out of reach of children

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

  • Directions

    Reverse cardboard sleeve then crush at dot between thumb and forefinger. Once solution has saturated tip, apply topically to the sting or bit. May be used on affected area(s) up to 4 times per day

    Not for use with children less than 2 years old without medical advise.

  • Other Information

    Store at room temperature 15º-30ºC (59º-86ºF) away from light.

  • Inactive Ingredients

    D&C Green Dye #5, D&C Yellow Dye #10, FD&C Blue Dye #1, Isopropyl Alcohol, PEG 300 NF, Purified Water USP

  • Label

    1407 BX MASTER1407 Medicaine Sting and Bite Ampule

  • INGREDIENTS AND APPEARANCE
    MEDICAINE STING AND BITE 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-405
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.12 g  in 0.6 mL
    Inactive Ingredients
    Ingredient NameStrength
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-405-0350 in 1 CASE02/14/1976
    1NDC:67777-405-0210 in 1 BOX
    1NDC:67777-405-016 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/14/1976
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124529)
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