STING AND BITE- benzocaine swab

Sting and Bite by

Drug Labeling and Warnings

Sting and Bite by is a Otc medication manufactured, distributed, or labeled by PHOENIX HEALTHCARE SOLUTIONS, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzocaine, 6% w/v

Purpose

Topical Analgesic

Use

For temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes and insect bites or minor skin irritations.

Warnings

• For external use only.

• Flammable, keep away from fire or flame

• Avoid contact with eyes; if this happens, rinse thoroughly with water

Do Not Use

With electrocautery procedures.

Stop Use

If irritation and redness develop.If condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days,discontinue use and consult a doctor.

Caution: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 age and older, apply to affected area not more than 3-4 times daily.
• For children under 2 years of age, consult a doctor before use.

Other information

Store at room temperature 150 -300 C (590 - 860 F). Avoid excessive heat.

Inactive ingredients

Isopropyl Alcohol, Purified Water

Principal Display Panel

NDC: 60913-031-01

Phoenix Healthcare Solutions, LLC

"An Innovative Medical Manufacturer"

Sting and Bite Pads

Medium

For Individual,Professional and Hospital Use

Saturated with 6% Benzocaine as a topical analgesic

Latex Free

100 Individual Pads

INGREDIENTS AND APPEARANCE

STING AND BITE 
benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60913-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60913-031-01	100 in 1 CARTON	02/23/2015
1		1 mL in 1 PACKET; 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	02/23/2015

Labeler - PHOENIX HEALTHCARE SOLUTIONS, LLC (079146847)