Label: EQUATE BURN RELIEF- lidocaine hydrochloride gel

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

Drug Label Information

Updated November 15, 2023

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  • ACTIVE INGREDIENT

    Active ingredient

    Lidocaine HCI         0.5%

  • PURPOSE

    Purpose

    External analgesic

  • INDICATIONS & USAGE

    Uses

    for the temporary relief of pain and itching associated with 

    • minor burns 
    • sunburn 
    • minor cuts 
    • scrapes
    • insect bites
    • minor skin irritations
  • WARNINGS

    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 eyes

    Stop use and ask a doctorif condition worsens, or if symptoms persist for more than 7 days or clearup and occur 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 right away.

  • DOSAGE & ADMINISTRATION

    Directions 

    • adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • INACTIVE INGREDIENT

    Inactive ingredients

    Aloe Barbadensis Leaf Juice, Blue 1, Carbomer, Disodium EDTA, Ethylhexylglycerin, Glycerin, Maltodextrin, Menthol, Phenoxyethanol, Polysorbate 20, Propanediol, SD Alcohol, Sodium Hydroxide, Water, Yellow 5

  • PRINCIPAL DISPLAY PANEL

    image description

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    EQUATE BURN RELIEF 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-237
    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
    WATER (UNII: 059QF0KO0R)  
    ALOE (UNII: V5VD430YW9)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CARBOMER 934 (UNII: Z135WT9208)  
    DISODIUM HEDTA (UNII: KME849MC7A)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    MENTHOL (UNII: L7T10EIP3A)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-237-08226 g in 1 BOTTLE; Type 0: Not a Combination Product11/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/15/2023
    Labeler - Walmart Inc (051957769)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nantong Health & Beyond Hygienic Products Inc.421280161manufacture(79903-237)
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