FDA Label for Medifirst Burn

View Indications, Usage & Precautions

Medifirst 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



Burn Spray

Pain Relief

Drug Facts


Active Ingredient



Lidocaine HCl 2.0%


Purpose



Topical pain relief


Uses



Temporary pain relief associated with minor burns


Warnings



For external use only


Do Not Use



  • In large quantities, particularly over raw or blistered areas
  • near eyes, if this happens rinse thoroughly with water

Otc - Stop Use



Stop use and ask doctor if condition worsens or persists for more than 7 days or clears up and returns


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.


Directions



  • spray an even layer of burn spray over cleaned affected area not more than 3-4 times daily
  • not to be used on children under 12 years of age

Inactive Ingredients



aloe vera, germaben II, propylene glycol, purified water


Questions Or Comments?



1-800-634-7680


Principal Display Panel - Bottle Label



MEDI-FIRST ®

Burn Spray

Pump Spray

Analgesic

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