Label: STINGX- benzocaine swab

  • NDC Code(s): 65753-350-15, 65753-350-16, 65753-350-17
  • Packager: CoreTex Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 22, 2023

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  • Active Ingredients

    Benzocaine 6%

  • Purpose

    Topical Analgesic

  • Use

    For temporary pain relief from insect bites and stings

  • Warnings

    For external use only

    Do Not Use

    • in or near eyes
    • over large areas of the body
    • over raw or blistered areas

    Stop use and aska doctor if

    • conditions worsen or persist for more than 7 days or clear up and occur again within a few days
  • Keep out of reach of children

    If swallowed get medical help or contact Poison Control center right away.

  • Directions

    Apply to affected area not more than 3 to 4 times daily, for adults and children 2 years of age or older.

  • Inactive Ingredients

    allantoin, glycerin, SD alcohol 40, water (aqua)

  • OTHER SAFETY INFORMATION

    Made in USA for CoreTex Products, Inc.

    Erwin, TN 37650 / www.CoreTexProducts.com

    (877)684-5774

  • Principal Display Panel

    350

  • INGREDIENTS AND APPEARANCE
    STINGX 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65753-350
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    ALLANTOIN (UNII: 344S277G0Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-350-1525 in 1 CONTAINER11/25/2019
    11.1 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:65753-350-1650 in 1 CONTAINER11/25/2019
    21.1 mL in 1 POUCH; Type 0: Not a Combination Product
    3NDC:65753-350-17300 in 1 CONTAINER11/25/2019
    31.1 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/25/2019
    Labeler - CoreTex Products Inc (061944620)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmetic Enterprises017701475manufacture(65753-350)
    Establishment
    NameAddressID/FEIBusiness Operations
    CoreTex Products Inc061944620pack(65753-350)
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