Label: FIRST AID BURN CREAM cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 19, 2024

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  • Active Ingredient

    Lidocaine Hydrochloride 0.5%

  • Purpose

    Topical Analgestic

  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Topical Antiseptic

  • Use(s)

    • For the temporary relief of pain and itching associated with:

    • Sunburn • Minor burns • Insect bites • Minor skin irritations • Cuts • Scrapes

  • Warnings

    For External Use Only

    Do not use

    • In the eyes • Over large areas of the body or on deep puncture wounds, animal bites, or serious burns

    • In large quantities, particularly over raw surfaces or blistered areas

    Stop use and aks a doctor if

    • The condition get worse • Condition clears up and recurs within a few days • Condition persists for more than 7 days

    If pregnant or breast feeding

    Ask a health care prfessional before use.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    Adults and children 2 years and over:

    • Clean the affected area

    • Apply a small amount of this product on the area 3 to 4 times daily

    • May be covered with a sterile bandage

    Children under 2 years: • Consult a doctor

  • Other Information

    • Store in a cool, dry area 15º-25ºC (59º-77ºF)

    • Tamper evident sealed packets

    • Do not use any opened or torn packets

  • Inactive Ingredients

    Butylated Hydroxytoluene, Cetomacrogol 1000, Cetostearyl Alcohol, Dimethicone, Glycerine, Glyceryl Monostearate, Isopropyl Myristate, Methylcellulose, Purified Water, Sodium EDTA, Sodium Methylparaben, Sodium Propylparaben

  • Questions?

    1-888-900-2920 Monday - Friday 8AM-4PM PST

  • Label

    FL-2044_BX_MASTERFL-2044

  • INGREDIENTS AND APPEARANCE
    FIRST AID BURN CREAM 
    first aid burn cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58228-6244
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS50 mg  in 10000 mg
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 10000 mg
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
    CETETH-20 (UNII: I835H2IHHX)  
    METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYLCELLULOSE (4000 MPA.S) (UNII: MRJ667KA5E)  
    DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58228-6244-11800 in 1 CASE01/26/2024
    125 in 1 BOX
    1900 mg in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/26/2024
    Labeler - Front Line Safety (061263699)
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