Label: STING RELIEF- benzocaine, isopropyl alcohol patch

  • 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 December 28, 2017

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  • Drug Facts

  • Active Ingredient

    Benzocaine, 6% w/w

    Isopropyl Alcohol, 60% v/v

    Purpose

    Topical Anesthetic

    Antiseptic

  • Use:

    For temporary relief of pain and itching associated with minor insect stings and bites.

  • Warnings:

    • Flammable, keep away from fire or flame

    Do not use:

    • in the eyes
    • if contact occurs, flush with water

    Stop use:

    • if irritation and redness develop. If condition persists consult your health care practitioner.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    For adults and children 2 years of older, apply to affected area 3 to 4 times daily. For children under 2 years of age, consult a physician before use.

  • Inactive Ingredient:

    Purified Water

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    STING RELIEF 
    benzocaine, isopropyl alcohol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71622-002
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71622-002-001 in 1 POUCH07/25/2017
    10.42 g 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 not finalpart333A07/25/2017
    Labeler - MCL Enterprises (784754173)
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