Label: BENZOCAINE- medicaine swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated September 2, 2021

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  • ACTIVE INGREDIENT

    Active Ingredients (each swab)

    Benzocaine USP (20%)

    L‐Menthol USP (1%)

  • PURPOSE

    Purpose

    Analgesic

  • INDICATIONS & USAGE

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

  • WARNINGS

    Warnings

    For external use only

    • do not use in the eyes
    • not for prolonged use
    • do not apply other medications to the same affected areas unless advised by a doctor
  • STOP USE

    Stop use and ask a doctor if condition for this preparation is used persists, or if a rash, irritation or allergic reaction develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.
    Not for use with children less than 2 years old without medical advice.
    If swallowed, get medical help immediately or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

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

  • OTHER SAFETY INFORMATION

    Other Information Store at room temperature away from light.

  • INACTIVE INGREDIENT

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

  • QUESTIONS

    Questions? Call 1-800-777-4908

  • PRINCIPAL DISPLAY PANEL

    NDC 68599-9560-1

    McKesson

    Medicaine Swabs

    Sting and Bite Relief

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

    Net Contents

    0.02 fl oz

    (0.6 mL)

    MFR# 15991

    15591 boxdrug factscase

  • INGREDIENTS AND APPEARANCE
    BENZOCAINE 
    medicaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-9560
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL1 mg  in 1 g
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68599-9560-10.21 g in 1 BOX; Type 0: Not a Combination Product01/16/202006/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/16/202006/01/2024
    Labeler - McKesson (023904428)
    Establishment
    NameAddressID/FEIBusiness Operations
    James Alexander Corp.040756421manufacture(68599-9560)
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