Label: BE SMART GET PREPARED STING RELIEF WIPE- alcohol, lidocaine hydrochloride liquid

  • NDC Code(s): 55550-201-03
  • Packager: Total Resources International, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 4, 2024

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  • Active Ingredients

    Ethyl alcohol 56.6% v/v

    Lidocaine HCl 2.0% w/w

  • Purpose

    First Aid Antiseptic

    Topical Analgesic

  • Uses

    First aid to help prevent infection in minor scrapes and temporary relief of itching of insect bites

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

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

    Stop use and ask 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 a Poison Control Center right away

  • Directions

    Adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily. Children under 2 years of age: Consult a doctor.

  • Inactive ingredients

    benzalkonium chloride, menthol, purified water

  • Principal Display Panel – 0.8 g Pouch Label

    BE SMART®

    GET PREPARED

    STING RELIEF
    WIPE

    DO NOT FLUSH

    SINGLE USE

    Temporary Relief from Stings & Bites

    Made in USA • Manufactured forTotal Resources Inti. Inc.

    Walnut, California 91789 • www.besmartgetprepared.com

    00-BEE-90103 Rev.03 • NDC 55550-201 -03

    1PC

    Principal Display Panel – 0.8 g Pouch Label
  • INGREDIENTS AND APPEARANCE
    BE SMART GET PREPARED STING RELIEF WIPE 
    alcohol, lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55550-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol0.566 mL  in 1 mL
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) Lidocaine Hydrochloride Anhydrous20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    benzalkonium chloride (UNII: F5UM2KM3W7)  
    menthol (UNII: L7T10EIP3A)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55550-201-031 mL in 1 PACKET; Type 0: Not a Combination Product05/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/20/2022
    Labeler - Total Resources International, Inc (790160535)
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