Label: MEDI-FIRST STING RELIEF- benzocaine 6%, isopropyl alcohol 60% swab

  • NDC Code(s): 47682-234-12, 47682-234-99
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 17, 2024

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  • Drug Facts

  • Active ingredient

    Benzocaine 6% w/v

    Isopropyl alcohol 60% w/v

  • Purpose

    Topical anesthetic

    Antiseptic

  • Uses

    For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

    • in the eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if

    • irritation, redness or other symptoms develop
    • 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

    Adults and children 2 years of age and older: Apply to affected area 3-4 times daily.

    Children under 2 years: CXonsult physician.

  • Other information

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

    purified water

  • Questions or comments?

    1-800-634-7680

  • Medi-First Sting Relief Wipes Label

    Medi-First®

    Sting Relief Wipes

    Benzocaine/ Isopropyl Acohol

    Topical Anesthetic/ Antiseptic

    Product # 23112

    NET CONTENTS: 10 wipes per box

    Mf StingRelief Wipes Label

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST STING RELIEF 
    benzocaine 6%, isopropyl alcohol 60% swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-234
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE60 mg  in 1 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.6 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-234-990.6 mL in 1 PACKET; Type 0: Not a Combination Product07/02/2018
    2NDC:47682-234-1210 in 1 BOX07/02/2018
    20.6 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/02/2018
    Labeler - Unifirst First Aid Corporation (832947092)
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