Label: MEDIFIRST BURN- lidocaine hydrochloride spray

  • NDC Code(s): 47682-225-02, 47682-225-17
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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  • 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

  • INGREDIENTS AND APPEARANCE
    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 DrugM01504/12/2013
    Labeler - Unifirst First Aid Corporation (832947092)
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