Label: OP FIRST AID SERIES INSECT STING RELIEF PAD- benzocaine, isopropyl alcohol cloth

  • NDC Code(s): 72459-013-01
  • Packager: Yiwu Ori-Power Medtech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • Drug Facts

  • Active Ingredients

    Benzocaine,6% w/v

    Isopropyl Alcohol,60% v/v

    Purpose

    Topical Anesthetic

    Antiseptic

  • Use

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

  • Warnings

    • For external use only.

    Do not use

    On broken skin,deep puncture wounds.Avoid contact with eyes. If happens,rinse thoroughly with water.

    Stop use

    If unusual redness,swelling,irritation or other symptoms occur,consult a physician immediately.

    Keep out of reach of children

    If swallowed,get medical help or contact a poison control center right away.

  • Directions

    • Apply to affected area not more than 3 to 4 times daily. for adults and children 2 years or older.
    • Children under 2years:consult physician.
  • Other information

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

  • Inactive ingredients

    Purified water,Sodium Bicarbonate.

  • Package Labeling:

    updated label

  • INGREDIENTS AND APPEARANCE
    OP FIRST AID SERIES INSECT STING RELIEF PAD 
    benzocaine, isopropyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72459-013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE60 mg  in 1 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.6 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72459-013-011 in 1 POUCH11/03/2020
    10.4 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/03/2020
    Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)
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