Label: SOOTH-A-STING- benzocaine, isopropyl alcohol swab

  • NDC Code(s): 50332-0048-1, 50332-0048-7
  • Packager: HART Health
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 18, 2024

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  • Active Ingredients

    Benzocaine 6%

    Isopropyl Alcohol 60%

  • Purpose

    Topical Anesthetic

    Topical Antiseptic

  • Uses

    Temporarily relief of pain and itching associated with

    • insect bites
    • insect stings
  • Warnings

    For external use only

    do not get in eyes

    not for prolonged use

    FLAMMABLE keep away from heat and flame

    Allergy alert: A severe allertic reaction to insect bites and stings may require life support measures. In such cases, immediately call 911 or your local emergency provider.

  • Do not use

    • more than 3 to 4 times daily
    • in or near the eyes or over large portions of the body
  • Stop use and ask a doctor if

    • symptoms last more than 3 days
    • unusual redness, swelling, rash, or other irriation occurs
  • Keep out of reach of children

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

  • Directions

    Adults and chldren 2 years of age and older:

    • remover stinger carefully
    • gently wipe on and around point of insect puncture
    • do not reuse wipe
    • dispose of wipe properly

    Children under 2 years of age:

    • ask a doctor
  • Inactive Ingredient

    Water

  • PRINCIPAL DISPLAY PANEL

    5337StingWipev21f.jpg

  • INGREDIENTS AND APPEARANCE
    SOOTH-A-STING 
    benzocaine, isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0048
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE.06 g  in 1 g
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL.60 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50332-0048-110 in 1 BOX04/01/1974
    1.35 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:50332-0048-7100 in 1 PACKAGE04/20/2016
    2.35 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM04/01/1974
    Labeler - HART Health (069560969)
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