Label: LIDOCAINE PAIN RELIEF GEL-PATCH patch

  • NDC Code(s): 84732-082-01
  • Packager: Dongguan Haiyi Technology Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 4, 2024

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  • Active ingredients

    Lidocaine 4%

  • Inactive ingredients

    Glycerin, Sodium Polyacrylate,Dihydroxyaluminum Aminoacetate,Disodium EthylenediaminetetraaceticAcid, Kaolin, Titanium Dioxide,Poly-sorbate 80, Propylene Glycol, TartaricAcid, Polyacrylic Acid,Polyvinylpyrroli-done K90, Methylparaben,Propylpara-ben, Water.

  • Purpose section

    Desensitizes AggravatedNerves And Relieves Pain :

    No lrritation

    Stay-put Flexible Patch

    Numbs Pain Away

  • Warning

    For external use only

  • stop use

    on wounds or damaged skin

    with a heating pad or devic

    with other ointments, creams,sprays, or liniments

    if your are allergic to any ingredients of this product

  • not use

    Not suitable for use by children, pregnantor breast feeding people.

  • Keep out of reach of children.

    If swallowed accidentally , get medical help or contact with Poison Control Center immediately.

  • HOW TO USE

    Adults and Children above 12 year sold:
    Clean and dry the affected area.

    Tear off the protective film andapply the exposed part of the patch tothe affected area.

    Carefully remove remaining film while pressing the patch firmly on theskin.patch firmly on the skin.

    Remove patch from the skin afterat most 8-hour application

  • Dosage

    take an appropriateamount,Use 2-3 times a week

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    LIDOCAINE PAIN RELIEF GEL-PATCH 
    lidocaine pain relief gel-patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84732-082
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 mg  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TARTARIC ACID (UNII: W4888I119H)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    KAOLIN (UNII: 24H4NWX5CO)  
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84732-082-0170 g in 1 BOX; Type 0: Not a Combination Product11/04/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/04/2024
    Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dongguan Haiyi Technology Co.,Ltd.722030807manufacture(84732-082)
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