Label: SOOTH-A-STING- benzocaine swab

  • NDC Code(s): 50332-0050-0, 50332-0050-4
  • Packager: HART Health
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 18, 2024

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  • Active Ingredients

    Benzocaine 20%

    L-Menthol 1%

  • Purpose

    Topical Anesthetic

    Topical Anesthetic

  • 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

    Allergy alert: A severe allertig 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

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

    • condition persists
    • unusual redness, swelling, rash, or irritation 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

    • remove stinger carefully
    • reverse cardboard sleeve
    • crush tube between thumb and forefinger to release fluid
    • apply on and aroundpoint of insect puncture
    • do not reuse swab
    • dispose of swab properly
  • Inactive Ingredient

    D&C green dye#5, D&C yellow dye #10, FD&C blue dye #1, PEG 300 NF, isopropyl alcohol, purified water USP

  • PRINCIPAL DISPLAY PANEL

    0440StingSwab23f.jpg0440StingSwab23f.jpg

  • INGREDIENTS AND APPEARANCE
    SOOTH-A-STING 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.12 g  in 0.6 mL
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM.006 g  in 0.6 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50332-0050-010 in 1 BOX01/01/2000
    1.6 mL in 1 AMPULE; Type 0: Not a Combination Product
    2NDC:50332-0050-4100 in 1 BAG01/01/2000
    2.6 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01/01/2000
    Labeler - HART Health (069560969)
    Registrant - HART Health (069560969)
    Establishment
    NameAddressID/FEIBusiness Operations
    JAMES ALEXANDER CORPORATION040756421manufacture(50332-0050)
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