FDA Label for Medi-first Protective Coating Bandage
View Indications, Usage & Precautions
Medi-first Protective Coating Bandage Product Label
The following document was submitted to the FDA by the labeler of this product Unifirst First Aid 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 3.2% w/w
Purpose
Topical antiseptic
Topical anesthetic
Uses
First aid to help protect against infection in
minor cuts and scrapes
burns
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 eyes or other mucus membranes
in case of serious burns
in case of deep or puncture wounds
for a prolonged period of time
on a large portion of the body
Stop Use And Ask A Doctor If
condition worsens or symptoms persist for more than 7 days
condition clears up and recurs within a few days
redness, swelling, or irritation occurs
Directions
clean the affected area
shake can well before using
hold 4-6 inches from surface and spray area until wet
may be covered with sterile bandage. If bandaged, let dry first
for adult institutional use only
not intended for use on children
Other Information
avoid inhaling
use only as directed
intentional misuse by deliberately concentrating and inhaling contents may be harmful or fatal
Inactive Ingredients
Ethyl alcohol, isobutane, n-butane, propane, PVP-VA copolymer
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