STINGEZE INSECT BITE RELIEF- benzocaine, phenol, camphor liquid

StingEze by

Drug Labeling and Warnings

StingEze by is a Otc medication manufactured, distributed, or labeled by Wisconsin Pharmacal Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients                                                         Purpose

Benzocaine 5%...........................................................................Analgesic, Anesthetic, Antipuritic

Phenol 1.35%.............................................................................First Aid Antiseptic

Camphor 3.0%............................................................................External Analgesic

Purpose

Analgesic, Anesthetic, Antipuritic

First Aid Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

When using this product

• Do not get in eyes
• Do not apply over large areas of the body
• In case of deep or puncture wounds, animal bites, or serious burns consult a doctor
• Do not bandage.
  

Stop use and ask doctor if

condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days.  Do not use longer than one week unless directed by a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.  If in eyes, flush with water for 15 minutes and call a physician.

Directions

• Clean area
• Apply a small amount to the bite area while massaging with sponge tip applicator.  If itching persists, apply again in 10-15 minutes
• For ticks and bees, remove tick or stinger before treatment
• Adults and children 2 years and over: Apply to affected area 1 to 3 times daily
• Children under 2 years: Consult a doctor
  

Inactive Ingredients

Propylene Glycol

Questions or Comments?

1-800-558-6614

PRINCIPAL DISPLAY PANEL

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PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

STINGEZE  INSECT BITE RELIEF
benzocaine, phenol, camphor liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68093-7038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5)	Benzocaine	0.05 g  in 1 g
Phenol (UNII: 339NCG44TV) (Phenol - UNII:339NCG44TV)	Phenol	0.0135 g  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	0.03 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Propylene Glycol (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68093-7038-1	1 in 1 CARTON
1		14.79 g in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/01/2009

Labeler - Wisconsin Pharmacal Company (800873986)

Establishment
Name	Address	ID/FEI	Business Operations
Wisconsin Pharmacal Company		800873986	manufacture(68093-7038)