Label: MEDI-FIRST PLUS BURN WITH LIDOCAINE- benzalkonium chloride, lidocaine cream
MEDI-FIRST BURN WITH LIDOCAINE- benzalkonium chloride, lidocaine cream

  • NDC Code(s): 47682-270-12, 47682-270-73, 47682-270-99, 47682-930-73
  • 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

    Active ingredients

    Benzalkonium chloride 0.13%

    Lidocaine HCl 0.5%

  • PURPOSE

    Purposes

    First aid antiseptic

    External analgesic

  • INDICATIONS & USAGE

    Uses

    first aid to help prevent infection and for the temporary relief of pain and itching associated with

    • minor cuts
    • scrapes
    • burns
  • WARNINGS

    Warnings

    For external use only.

  • DO NOT USE

    Do not use

    • in the eyes or apply over large areas of the body
    • longer than 1 week unless directed by a doctor
    • in large quantities, particularly over raw surfaces or blistered areas
  • ASK DOCTOR

    Ask a doctor before use if you have

    deep or puncture wounds, animal bites or serious burns

  • WHEN USING

    When using this product avoid contact with the eyes

  • 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
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions

    • adults and children 2 years of age and older:
      • clean the affected area
      • apply a small amount of this product on the area 1 to 3 times daily
      • may be covered with a sterile bandage

    • children under 2 years of age: consult a doctor
  • OTHER SAFETY INFORMATION

    Other information

    • store at room temperature
    • tamper evident. Do not use if packet is opened or torn
    • you may report a serious adverse reaction to this product to 800-634-7680

  • INACTIVE INGREDIENT

    Inactive ingredients

    aloe barbadensis leaf juice, cetyl alcohol, diazolidinyl urea, disodiun EDTA,, glycerin, glyceryl stearate SE, methylparaben, mineral oil, PEG 100, propylene glycol, propylparaben, stearic acid, triethanolamine, water

  • QUESTIONS

    Questions or comments? 1-800-634-7680

  • PRINCIPAL DISPLAY PANEL

    Medi-First®

    Burn Cream with Lidocaine

    Benzalkonium Chloride 0.13% / First Aid Antiseptic

    Lidocaine HCl 0.5% / External Analgesic

    Product # 20669

    10 Units Net Wt 0.9 g (1/32 oz)

    20669

  • PRINCIPAL DISPLAY PANEL

    Medi-First® Plus

    Burn Cream with Lidocaine

    Benzalkonium Chloride 0.13% / First Aid Antiseptic

    Lidocaine HCl 0.5% / External Analgesic

    25 Units of 0.9 g Packets

    Item #93973

    93973

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST PLUS BURN WITH LIDOCAINE 
    benzalkonium chloride, lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-930
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-930-7325 in 1 BOX03/11/202104/30/2028
    10.9 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/11/202104/30/2028
    MEDI-FIRST BURN WITH LIDOCAINE 
    benzalkonium chloride, lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-270
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-270-7325 in 1 BOX06/01/202104/30/2028
    10.9 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-270-1210 in 1 BOX06/01/202104/30/2028
    20.9 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-270-990.9 g in 1 PACKET; Type 0: Not a Combination Product06/01/202104/30/2028
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/01/202104/30/2028
    Labeler - Unifirst First Aid Corporation (832947092)
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