Label: 2.0% LIDOCAINE BURN- lidocaine hydrochloride spray

  • NDC Code(s): 52000-441-02
  • 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 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 area • near eyes, if this happens rinse thoroughly with water

    ​Stop use and ask a doctor if ​the 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

    AMINOMETHYL PROPANOL, GLYCERIN, HYDROXYPROPYL METHYLCELLULOSE, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, OCTOXYNOL-9, PEG-40 HYDROGENATED CASTOR OIL, PHENOXYETHANOL, PROPYLENE GLYCOL, WATER

  • SPL UNCLASSIFIED SECTION

    ✓ Instant Cooling Relief

    ✓ Soothes Minor Burns & Sunburns

    Store at 68°-77°F (20°-25°C)

    ​Mfd for and Distributed by:
    Universal Distribution Center LLC
    330 Applegarth Road,
    Monroe Township, NJ 08831

    www.universaldc.com

    MADE IN CHINA

  • Packaging

    2.0%LIDOCAINEBURN

  • INGREDIENTS AND APPEARANCE
    2.0% LIDOCAINE BURN 
    lidocaine hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-441
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    OCTOXYNOL-9 (UNII: 7JPC6Y25QS)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-441-0259.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/19/2026
    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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