FDA Label for Medi-first Burn
View Indications, Usage & Precautions
Medi-first Burn 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.
Other
Drug Facts
Otc - Active Ingredient
Active ingredient
Lidocaine HCl 2.0%
Otc - Purpose
Purpose
External analgesic
Indications & Usage
Uses
for the temporary relief of pain associated with minor burns
Warnings
Warnings
For external use only.
Otc - Do Not Use
Do not use in large quantities, particularly over raw or blistered areas
Otc - When Using
When using this product avoid contact with eyes
Otc - Stop Use
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days
- condition clears up and occurs again within a few days
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions
- 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 doctor
Other Safety Information
Other information
- store at room temperature
- you may report a serious adverse reaction to this product to 1-800-634-7680
Inactive Ingredient
Inactive ingredients
diazolidinyl urea, edetate disodium, glycerin, hypromellose, methylparaben, octoxynol 9, propylene glycol, propylparaben, tea tree oil, trolamine, water
Otc - Questions
Questions or comments? 1-800-634-7680
Package Label.Principal Display Panel
Medi-First®
Burn Spray
Pump Spray
Lidocaine HCl 2.0%
Topical Analgesic
Relieves pain in monor burns
Store at room temperature
2 FL OZ (59.1 ML)
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