Label: STING-KILL- benzocaine and menthol solution

  • 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 February 13, 2017

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  • Active ingredients

    Benzocaine USP 20%

    Menthol USP 1%

  • Purpose

    (for pain) Topical Anesthetic

    (anti-itch) Antipruritic

  • Keep Out of Reach of Children

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

  • Uses

    Temporarily relieves pain and itching of bee stings, insect bites and minor skin irritations.
  • Warnings

    For external use only
    Avoid contact with eyes

    Get medical help right away if

    You are sensitive to insect venom. You may develop a serious reaction when stung.

    Stop use and ask a doctor if

    Condition worsens
    Symptoms last for more than 7 days
  • Directions

    Children under 2 yrs.

    Do not use
    Consult doctor

    Adults and children 2 yrs. and older

    Apply to affected area as needed but not more than 3 to 4 times a day.
    (1) Bee stings only, remove stinger before treatment.
    (2) Tear foil pack at notch, exposing pad.
    (3) Apply immediately to bite or sting area. Dispose of pad after use.
  • Inactive Ingredients

    FD&C Blue #1, FD&C Yellow #5, Isopropyl Alcohol 15%, PEG-8, Water.

  • Package/Label Principal Display Panel

    #1 CHOICE OF PHARMACISTS

    2 in 1 FORMULA

    STING-KILL®

    Kills the Pain and Stops the Itch with MAXIMUM STRENGTH Benzocaine and Menthol

    For fast relief from:

    Bee Stings • Mosquito Bites

    Insect Bites • Jellyfish

    MADE IN THE USA

    EXTERNAL ANESTHETIC WIPES

    SANITARY• CONVENIENT

    8 DISPOSABLE SATURATED WIPES

    carton-label
  • INGREDIENTS AND APPEARANCE
    STING-KILL 
    benzocaine and menthol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52412-250
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorBLUE (Blue) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52412-250-208 in 1 BLISTER PACK01/01/1965
    10.56 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:52412-250-218 in 1 CARTON01/15/2017
    20.56 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34801/01/1965
    Labeler - Randob Ltd. (061995007)
    Registrant - Randob Ltd. (061995007)