Label: LIDOZALL- lidocaine hydrochloride cream

  • NDC Code(s): 72835-004-01, 72835-004-20
  • Packager: V2 Pharma LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2024

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  • Lidozall 

    Rapid-onset topical analgesic

    Lidozall should be administered under the supervision of a licensed medical practitioner.

  • Active Ingredients

    Lidocaine HCL 4.0% w/w

    Purpose

    External analgesic

  • Uses

    For temporary relief of pain and itching due to minor skin irritations.

  • Warnings

    - For external use only.
    - Avoid contact with eyes.

  • DO NOT USE

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

  • STOP USE

    - 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. Discontinue use.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    For adults and children two-years or older: Apply 1 packet (2 grams) topically to the affected area(s) up to 4 times daily as needed for pain. Do not use more than 4 packets (8 grams) per day.

  • Inactive Ingredients

    Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmenthane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.

  • Other Information

    Protect this product from excessive heat and direct sun.

  • Product Label

    Packaging for Lidozall is shown below: 

    Lidozall 2 Gram Packet

    NDC 72835-004-01

    Lidozall Packet

    Lidozall Box of 20 Count, 2 Gram Packets

    NDC 72835-004-20

    Lidozall Box of 20 Packets

  • INGREDIENTS AND APPEARANCE
    LIDOZALL 
    lidocaine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72835-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    WATER (UNII: 059QF0KO0R)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    EMU OIL (UNII: 344821WD61)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72835-004-2020 in 1 CARTON12/16/2024
    1NDC:72835-004-012 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/21/2024
    Labeler - V2 Pharma LLC (102457346)
    Establishment
    NameAddressID/FEIBusiness Operations
    V2 Pharma LLC102457346label(72835-004) , manufacture(72835-004) , pack(72835-004)
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