Label: STING RELIEF- benzocaine, isopropyl alcohol solution

  • NDC Code(s): 72459-282-00
  • Packager: Yiwu Ori-Power Medtech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 18, 2024

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  • DRUG FACTS

  • Active Ingredients

    Benzocaine 6% w/v, Isopropyl Alcohol 60% w/v

    Purpose

    For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites.

  • Inactive Ingredients

    Purified Water, Sodium Bicarbonate.

  • Use

    Temporary relief for minor burns, scrapes and insect bites.

  • Directions

    Apply to affected area no more than 3 to 4 times daily. For children under 2 years of age, consult physician before use.

  • Storage

    Store at room temperature 15°C - 30°C (59°F - 86°F).

  • Warnings

    Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If irritation develops, consult physician. Do not use on broken skin, deep puncture wounds.

    Keep Out Of Reach Of Children

    In case of accidental swallowing, seek medical help and contact poison control immediately.

    Do not use 

    on broken skin, deep puncture wounds.

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    STING RELIEF 
    benzocaine, isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72459-282
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE60 mg  in 1 g
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL600 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72459-282-000.34 g in 1 POUCH; Type 0: Not a Combination Product02/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/01/2024
    Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)
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