STING-KILL- benzocaine and menthol solution 
Randob Ltd.

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.

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Drug Facts

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
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)

Revised: 2/2017
Document Id: b6b84806-0cda-43ca-99ef-3eed522aa864
Set id: b6b84806-0cda-43ca-99ef-3eed522aa864
Version: 1
Effective Time: 20170213
 
Randob Ltd.