Label: MAXOCAINE LIDOCAINE HEMP OIL TOPICAL ANALGESIC- lidocaine hydrochloride solution

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

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active Ingredients

    Lidocaine hydrochloride 4%

    Purpose

    Topical Analgesic

  • Uses:

    For the temporary relief of pain and itching associated with minor burns, sunburns, minor cuts, scrapes, insect bites, or 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.

    If pregnant or breast-feeding.

    ask a health professional before use.

  • Directions:

    • Apply to affected area not more than 3 to 4 times daily. Adults and children 2 years of age and older: 
    • Consult a doctor. Children under 2 year of age:

  • Other Information:

    Store at 20-25°C (68-77°F) and protect from moisture.

  • Inactive ingredients

    Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cannabis Sativa (Hemp) Seed Oil, Carbomer, Dimethicone, Ethylhexylglycerin, Eucalyptus Globulus Oil, Ilex Paraguariensis (Yerba Mate) Extract, Isopropyl Myristate, Mentha Viridis (Spearmint) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, Triethanolamine.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    MAXOCAINE LIDOCAINE HEMP OIL TOPICAL ANALGESIC 
    lidocaine hydrochloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72188-188
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    SPEARMINT (UNII: J7I2T6IV1N)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72188-188-0030 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product04/24/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/24/2021
    Labeler - Prime Commerce, LLC (016785608)
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