Benzocaine by Dynarex Corporation BENZOCAINE swab

Benzocaine by

Drug Labeling and Warnings

Benzocaine by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient  Purpose  

Benzocaine, 6% w/v                       Topical Analgesic

Purpose for Benzocaine

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

Keep Out of Reach of Children

• Keep out of reach of children.
• If swallowed, get medical help or contact a Poison Control Center.
  

Indications and Usage

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

Warnings

Warnings: Benzocaine

• For external use only.
• Flammable, keep away from fire or flame.
  

Dosage

Directions:

• For adults and children 2 years of age and older, apply to affected area not more than 3-4 times daily.
• Children under 2 years; consult a physician.

Inactive Ingredients

• Inactive Ingredients: Isopropyl Alcohol, Water.
  

DO Not Use

Do not use:

With electrocautery procedures.

Stop Use

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.

Storage and Handling

• Avoid excessive heat.
• Store at room temperature: 15 - 30 degrees C (59 - 86 degrees F)
  

Principal Display Panel

Dynarex Sting and Bite

Benzocaine.jpg

INGREDIENTS AND APPEARANCE

BENZOCAINE 
benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-246
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	60 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-246-01	2 mL in 1 PACKET; Type 0: Not a Combination Product	07/20/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	07/20/2011

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)