Label: BE SMART GET PREPARED STING RELIEF WIPE- benzocaine, alcohol cloth

  • NDC Code(s): 55550-271-01
  • Packager: Total Resources International, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 16, 2024

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  • o Active Ingredients

    • Benzocaine 6% v/v
  • Purpose

    Local Anesthesia

  • • USES

    • Relieves stinging and itching caused by mosquito bites, minor burns, and abrasions
  • • WARNINGS

    • For external use only

    • Do not use
      • If allergic to certain ingredients
      • In eyes, mouth, and mucous membranes

    • Stop use and ask the doctor if condition worsens or persists for more than 7 days or clears up and occurs again within a few days

    • Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center.
  • • DIRECTIONS

    • Adults and children 2 years of age and older: tear open packet, unfold, and use as a washcloth. Allow hands to dry without wiping. Children under 2 years: Consult a physician
  • • INACTIVE INGREDIENT

    • water
  • Principal Display Panel

    BE SMART

    GET PREPARED®

    STING RELIEF WIPE 1 PC

    Do Not Flush

    Single Use

    Made in China

    Manufactured for Total Resources Intl. Inc.

    Walnut, California 91789

    www.besmartgetprepared.com • 00-BEE-90105COM Rev. 00

    NDC 55550-271-01

    Principal Display Panel
  • INGREDIENTS AND APPEARANCE
    BE SMART GET PREPARED STING RELIEF WIPE 
    benzocaine, alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55550-271
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55550-271-010.62 mL in 1 PACKET; Type 0: Not a Combination Product08/16/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/16/2024
    Labeler - Total Resources International, Inc (790160535)
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