Label: LIDOCAINE PAIN RELIEF GEL PATCH- lidocaine pain relief patch

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

Drug Label Information

Updated March 15, 2024

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  • Active Ingredients

    Lidocaine 4%

  • Puropose

    Topical anesthetic

  • Use

    For temporary relief of pain

  • Warnings

    For external use only

    Do not use

    • more than 1 patch at a time
    • on wounds or damaged skin
    • with a heating pad
    • if you are allergic to any ingredients of this product

    When using this product

    • use only as directed
    • avoid contact with the eyes, mucous membranes or rashes
    • do not bandage tightly

    Stop use and ask a doctor if

    • localized skin reactions, such as rash, itching, redness, pain, swelling and blistering develop
    • conditions worsen
    • symptoms persist for more than 7 days
    • symptoms clear up and occur again within a few days

    if pregnant or breast feeding

    ask a health professional before use

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children 12 years of age and over:

    • clean and dry affected area
    • remove film from patch and apply to the skin
    • apply 1 patch at a time to affected area, not more than 3 to 4 times daily
    • patch should not be applied longer than an 8 hour period

    Children under 12 years of age: consult a doctor

  • Other Information

    • Avoid storing product in direct sunlight
    • Protect product from excessive moisture

  • Inactive Ingredients

    Dihydroxyaluminum Aminoacetate, Glycerol, Kaolin, Methylparaben, Polyacrylic Acid (250000 MW), Polysorbate 80, Povidone K90, Propylene Glycol, Propylparaben, Sodium Polyacrylate (2500000 MW), Tartaric Acid, Titanium Dioxide, Water

  • Questions?

    1-888-DYNAREX

  • PRINCIPAL DISPLAY PANEL

    1454 BX Master

  • INGREDIENTS AND APPEARANCE
    LIDOCAINE PAIN RELIEF GEL PATCH 
    lidocaine pain relief patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    KAOLIN (UNII: 24H4NWX5CO)  
    TARTARIC ACID (UNII: W4888I119H)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-009-4060 in 1 CASE08/27/2019
    1NDC:67777-009-395 in 1 BOX
    140 mg in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/27/2019
    Labeler - Dynarex (008124539)
    Registrant - Dynarex (008124539)
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