STING-KILL- benzocaine and menthol solution

Sting-Kill by

Drug Labeling and Warnings

Sting-Kill by is a Otc medication manufactured, distributed, or labeled by Randob Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 not more than 3 to 4 times a day.
• ▪ (1) Bee stings only, remove stinger before treatment.
• ▪ (2) Remove strip of swabs from card. Push bottom of individual swab through paper backing.
• ▪ (3) Pop inner glass casing by squeezing plastic vial firmly between thumb and forefinger.
• ▪ (4) Hold swab so Sting-Kill formula saturates applicator tip.
• ▪ (5) Apply immediately to bite or sting area. Dispose of swab 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 SWABS SANITARY CONVENIENT

5 DISPOSABLE SWABS 1/2 cc EACH

INGREDIENTS AND APPEARANCE

STING-KILL 
benzocaine and menthol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52412-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	200 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-8 LAURATE (UNII: 762O8IWA10)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	BLUE (Blue)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52412-200-10	5 in 1 BLISTER PACK	01/01/1965
1		0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2	NDC: 52412-200-11	1 in 1 CARTON	01/15/2017
2		5 in 1 BLISTER PACK
2		0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
3	NDC: 52412-200-12	2 in 1 CARTON	01/01/1996
3		5 in 1 BLISTER PACK
3		0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/01/1965

Labeler - Randob Ltd. (061995007)

Registrant - Randob Ltd. (061995007)