MEDIFIRST BURN- lidocaine hydrochloride spray 
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Medi-First Burn Spray

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

Stop use and ask doctor if

condition worsens or persists for more than 7 days or clears up and returns.

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

Medi-First Burn Spray Label

MEDI-FIRST ®

Burn Spray

Pump Spray

Analgesic

  • Relieves pain in minor burns
  • Washable

2 FL OZ (59.1ML)

Principal Display Panel - Bottle Label

MEDIFIRST BURN 
lidocaine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-225
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
WATER (UNII: 059QF0KO0R)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-225-170.09 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/12/201304/02/2018
2NDC:47682-225-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/12/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/12/2013
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 10/2022
Document Id: ebdc8f15-5462-0bc8-e053-2995a90ac8f3
Set id: 9fa5b348-29c2-4cd0-a945-0486bd27f5e0
Version: 11
Effective Time: 20221025
 
Unifirst First Aid Corporation