Label: 0.5% LIDOCAINE BURN RELIEF- lidocaine hydrochloride gel

  • NDC Code(s): 52000-437-08
  • Packager: Universal Distribution Center LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2026

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  • Drug Facts

  • Active ingredient

    Lidocaine HCl 0.5%

  • Purpose

    External analgesic

  • Uses

    for the temporary relief of pain and itching associated with • minor burns • sunburn • minor cuts • scrapes • insect bites • minor skin irritations

  • Warnings

    For external use only

    Do not use in large quantities, particularly over raw surfaces or blistered areas

    When using this product avoid contact with the eyes

    Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

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

  • Directions

    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor

  • Other information

    Store a room temperature • Protect from direct sunlight.

  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Carbomer, Disodium EDTA, Ethylhexylglycerin, FD&C Blue NO.1, FD&C Yellow NO.5, Glycerin, Menthol, Maltodextrin, Propanediol, Polysorbate 20, Phenoxyethanol, Sodium Hydroxide, SD Alcohol, Water.

  • SPL UNCLASSIFIED SECTION

    ✓ Soothes & Cools Minor Burns

    ✓ Menthol Formula for Fast Pain Relief

    ✓ Helps Prevent Infection

    PAIN RELIEVING GEL WITH ALOE

    Mfd for and Distributed by:
    Universal Distribution Center LLC
    330 Applegarth Road, Monroe Township, NJ 08831
    www.universaldc.com

    MADE IN CHINA

  • Packaging

    0.5% LIDOCAINE BURN RELIEF

  • INGREDIENTS AND APPEARANCE
    0.5% LIDOCAINE BURN RELIEF 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-437
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-437-083 in 1 BOX01/19/2026
    1226 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/19/2026
    Labeler - Universal Distribution Center LLC (019180459)
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