Label: XEROBURN BURN GEL- lidocaine hydrochloride gel

  • NDC Code(s): 67777-129-00, 67777-129-01, 67777-129-02, 67777-129-03, view more
    67777-129-09, 67777-129-10, 67777-129-11
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 13, 2025

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  • Active Ingredient

    Lidocaine Hydrochloride 2%

  • Purpose

    Analgesic

  • Use(s)

    ■ For the temporary relief of pain associated with ■ Minor burns ■ Sunburn

    ■ Provides cooling pain relief

  • Warnings

    For External Use Only

    Do not use

    ■ On wounds or damaged skin

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

    When using this product

    ■ Avoid contact with the eyes

    ■ Do not bandage tightly

    Stop use and ask a doctor if

    ■ Condition worsens

    ■ Symptoms persist for more than 7 days

    ■ Symptoms 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 (1-800-222-1222) 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: Consult a doctor

  • Other Information

    • Store at room temperature 15º-30ºC (59º-86ºF)

    • Tamper Evident. Do not use if seal is damaged.

  • Inactive Ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosscopolymer, Carbomer, Glycerin, Imidazolidinyl Urea, Methylparaben, Propylene Glycol, Propylparaben, Purified Water, Tea Tree Leaf Oil, Triethanolamine

  • Questions?

    1-888-396-2739 Monday - Friday, 9AM - 5PM EST

  • Label

    1294_IN_MASTERXeroBurn Burn Gel

  • Label

    1290_BX_MASTERXeroBurn Burn Gel 1290

  • Label

    1291_BX_MASTERXeroBurn Burn Gel 1291

  • Label

    1292_MC_MASTERXeroBurn Burn Gel 1292

  • INGREDIENTS AND APPEARANCE
    XEROBURN BURN GEL 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-129
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    IMIDUREA (UNII: M629807ATL)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-129-10600 in 1 CASE09/07/2017
    1NDC:67777-129-016 in 1 BOX
    13.5 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:67777-129-09600 in 1 CASE09/07/2017
    2NDC:67777-129-0025 in 1 BOX
    23.5 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:67777-129-021728 in 1 CASE09/07/2017
    33.5 g in 1 PACKET; Type 0: Not a Combination Product
    4NDC:67777-129-1124 in 1 CASE09/07/2017
    4NDC:67777-129-03113 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01709/07/2017
    Labeler - Dynarex Corporation (008124539)
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