Label: LIDOCAINE AND MENTHOL patch

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

Drug Label Information

Updated November 3, 2025

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  • Active ingredients (in each patch)

    Lidocaine 4%

  • Purpose

    External Anesthetic

  • Active ingredients (in each patch)

    Menthol 1%

  • Purpose

    External Analgesic

  • Use

    Temporarily relieves minor pain

  • Warnings

    For external use only

    Do not use

    • more than one patch on your body at a time 
    • on cut, irritated or swollen skin 
    • on puncture wounds 
    • for more than one week without consulting a doctor 
    • if you are allergic to any active or inactive ingredients 
    • if pouch is damaged or opened

    When using this

    • use only as directed 
    • read and follow all directions and warnings on this carton 
    • do not allow contact with the eyes 
    • do not use at the same time as other topical analgesics 
    • do not bandage tightly or apply local heat (such as heating pads) to the area of use 
    • do not microwave 
    • dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

    Stop use and consult a doctor if

    • condition worsens 
    • redness is present 
    • irritation develops 
    • symptoms persist for more than 7 days or clear up and occur again within a few days 
    • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

    If pregnant or breastfeeding,

    ask a health professional before use.

    Keep out of reach of children and pets.

    If swallowed, get medical help or contact a Poison Control Center 1-800-222-1222 right away.

  • Directions

    Adults and children 12 years of age and over:clean and dry affected area, free of lotions, ointments, and creams. Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Do not use more than one patch in a 12-hour period. Maximum 2 patches per day. Discard patch after single use.
    Children under 12 years of age:consult a physician.

  • Other information

    Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

  • Inactive ingredients

    dihydroxyaluminum aminoacetate, edetate disodium, glycerin, hydroxyacetophenone, kaolin, mineral oil, polyacrylic acid, polysorbate 80, povidone K90, propylene glycol, sodium polyacrylate, tartaric acid, titanium dioxide, water

  • Questions or comments?

    Call (307) 410-3813 or email info@marcellahealth.com

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  • INGREDIENTS AND APPEARANCE
    LIDOCAINE AND MENTHOL 
    lidocaine and menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85096-101
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g  in 1 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.01 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    KAOLIN (UNII: 24H4NWX5CO)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85096-101-3030 in 1 CARTON11/03/2027
    11 in 1 POUCH
    110 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/24/2025
    Labeler - Marcella Health (119381899)
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