Label: BENZOCAINE swab

  • NDC Code(s): 67777-246-01, 67777-246-02, 67777-246-03, 67777-246-04
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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  • Active Ingredient

    Benzocaine, 6% w/v

  • Purpose

    Topical Analgesic

  • Active Ingredient

    Isopropyl Alcohol, 60% w/v

  • Purpose

    Antiseptic

  • Use(s)

    For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations.

  • Warnings

    For External Use Only

    • Flammable, keep away from fire or flame

    • Avoid contact with eyes; if this occures, rinse thoroughly with water

    • Do not use with electrocautery procedures

    Stop use if

    • Irritation and redness develop

    • Condition worsens or symptoms persists for more than 7 days, or clear up and occur again within a few days, discontinue use and consult a doctor

    Keep out of reach of children

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

  • Directions

    • For adults and children 2 years of age and older: Apply to affected area not more than 3-4 times daily.
    • Children under 2 years: Consult a physician before use
    • For other uses: Apply as needed

  • Other Information

    • Store at room temperature between 15º-30ºC (59º-86ºF)

    • Avoid excessive heat

  • Inactive Ingredients

    Water

  • Questions?

    1-888-396-2739 Monday - Friday 9AM-5PM EST.

  • Label

    1408 DM MasterSting & Bite Pad Label

  • Label 1408UB-10

    1408UB-10_BX_MASTER1408UB-10

  • INGREDIENTS AND APPEARANCE
    BENZOCAINE 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-246
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL60 mg  in 100 mL
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-246-023000 in 1 CASE07/20/2011
    1NDC:67777-246-012 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:67777-246-04480 in 1 CASE07/20/2011
    2NDC:67777-246-0310 in 1 BOX
    22 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/20/2011
    Labeler - Dynarex Corporation (008124539)
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