Label: STING RELIEF WIPES swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 4, 2024

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  • Active ingredients

    Benzocaine, 6% w/v

  • Purpose

    Topical Analgesic

  • Active Ingredient

    Isopropyl Alcohol, 60% w/v

  • Purpose

    Antiseptic

  • Use(s)

    For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations

  • Warnings

    For External Use Only

    Flammable. Keep away from fire or flame.

    When using

    • Avoid contact with eyes; if this occurs, rinse thoroughtly with water

    Do not use

    • With electrocautery procedures

    Stop use if

    • Irritation and redness develop

    • Condition worsens or symptoms persist for more than 7 days, or clear up and occur again within a few day; discontinue use and consult a doctor

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • For adults and children 2 years of age and older, apply to affected area not more than 3-4 times daily.

    • For children under 2 years of age, consult a doctor before use.

  • Other information

    • Store at room temperature 15º-30ºC (59º-86ºF)

    • Avoid excessive heat

  • Inactive Ingredients

    Water

  • Questions and Comments?

    1-888-900-2920 Monday-Friday, 8AM-4PM PST

  • Label

    PS-2204_BX_MASTER

  • INGREDIENTS AND APPEARANCE
    STING RELIEF WIPES 
    sting relief wipes swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58228-2204
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL60 mg  in 100 mL
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58228-2204-11000 in 1 CASE01/08/2024
    110 in 1 BOX
    12 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/08/2024
    Labeler - ProStat First Aid LLC (061263699)
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