FDA Label for Benzocaine And Benzethonium
View Indications, Usage & Precautions
Benzocaine And Benzethonium Product Label
The following document was submitted to the FDA by the labeler of this product Tender Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Benzethonium Chloride 0.2% w/w
Benzocaine 10% w/w
Purpose
Topical Antiseptic
Topical Anesthetic
Uses
For temporary relief of pain, treatment and helps prevent infection in
- minor cuts and scrapes
- insect bites
- minor skin irritations
Warnings
For external use only
Flammable:
- keep away from fire or flame
- contents under pressure
- do not puncture or incinerate container
- do not expose to temperatures above 120°F
Do Not Use:
- in or near mucous membranes
- on serious burns
- on deep puncture wounds
- for a prolonged period of time
- on a large portion of the body
Stop Use And Ask A Doctor If:
- redness, swelling, or irritation occurs
- infection occurs
- condition persists or worsens
- symptoms persists for more than 7 days
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- clean the affected area
- shake can well before using
- for adult institutional use only
- not for use on children
- hold 4-6 inches from surface and spray area until wet
- may be covered with sterile bandage. If bandaged, let dry first
Other Information
- avoid inhaling
- use only as directed
- intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal
Inactive Ingredients
Dipropylene Glycol, Isobutane, n-Butane, Propane
Label
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