Label: STING RELIEF WIPE- isopropyl alcohol and benzocaine swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 25, 2022

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  • Active Ingredients

    • Isopropyl Alcohol 60%
    • Benzocaine, 6% 
  • Purpose

    • First Aid Antiseptic
    • Topical Analgesic
  • Uses

    Use first aid to help prevent infection in minor scrapes and temporary relief 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 ask a 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 of age and older, apply to affected area not more than 3 times daily.
    • Children under 2 years; consult a physician.
  • Inactive Ingredient:

    purified water

  • PRINCIPAL DISPLAY PANEL

    First aid antiseptic
    Topical Analgesic

    NDC 53439-120-10 Cut Care Insect Bite Antiseptic & Pain Relieving Wipes First aid antiseptic Topical Analgesic Contents: 100 Pre-Moistened Wipes

  • INGREDIENTS AND APPEARANCE
    STING RELIEF WIPE 
    isopropyl alcohol and benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81417-124
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.6 g  in 1 g
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.06 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81417-124-011 in 1 PACKET03/24/2022
    11 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34803/24/2022
    Labeler - Sled Distribution, LLC (079772888)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sled Distribution, LLC079772888manufacture(81417-124)
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