Label: MEDI-FIRST BURN- lidocaine hydrochloride gel

  • NDC Code(s): 47682-477-69
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 17, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each gram)

    Lidocaine HCI 2.0%

  • Purpose

    Topical analgesic

  • Uses

    For the temporary relief of pain associated with minor burns.

  • Warnings

    For external use only.

    Do not use

    • in large quantities, particularly over raw or blistered areas

    When using this product

    • avoid contact with the eyes

    Stop use ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clears up and occurs again within a few days

    Keep out of the reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • adults & children 2 years and older: apply to affected area not more than 3 to 4 times daily
    • children under 2: consult a doctor
  • Inactive ingredients

    aloe vera, carbomer, germaben II, propylene glycol, purified water, menthol, triethanolamine, vitamin E acetate

  • Questions?

    Call 1-800-634-7680

    Mfg. for Medique Products, 17080 Alico Commerce Ct., Ste 1, Fort Myers, FL 33967

  • Medi-First Burn Gel Label

    Medi-First ®

    Burn Gel

    Lidocaine HCl / Topical Analgesic

    Product # 47769

    NET CONTENTS: 6 Units of 1/8 oz

    MF BurnGel

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST BURN 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-477
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    MENTHOL (UNII: L7T10EIP3A)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-477-696 in 1 BOX, UNIT-DOSE07/30/2014
    13.3 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01507/30/2014
    Labeler - Unifirst First Aid Corporation (832947092)
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