Label: LIDOCAINE PAIN RELIEF GEL-PATCH- lidocaine patch

  • NDC Code(s): 83602-158-01, 83602-158-15, 83602-158-16, 83602-158-20, view more
    83602-158-21, 83602-158-28, 83602-158-30, 83602-158-31, 83602-158-32, 83602-158-38, 83602-158-39, 83602-158-40, 83602-158-41
  • Packager: Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 5, 2025

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  • Active ingredients

    Lidocaine 4% ...... Purpose: Topical Analgesic

  • Purpose

    Topical Anesthetic

  • Uses

    Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

  • Warnings

    For external use only

  • Do not use

    • on wounds or damaged skin
    • with a heating pad or device
    • with other ointments, creams, sprays, or liniments
    • 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 ... if

    • skin reactions such as redness, swelling, blistering or other discomfort occur
    • symptoms persist for more than 7 days
  • ... ask a doctor if

    • skin reactions such as redness, swelling, blistering or other discomfort occur
    • symptoms persist for more than 7 days
  • If pregnant or breast-feeding

    ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    Adults and Children above 12 years old:

    • Clean and dry the affected area.
    • Tear off the proctive film and apply the exposed part of the patch to the affected area.
    • Carefully remove remaining film while pressing the patch firmly on the skin.
    • Remove patch from the skin after at most 8-hour application.

    Children under age of 12: Consult a doctor

  • Inactive Ingredients

    Dihydroxyaluminum Aminoacetate, Disodium Ethylenediaminetetraacetic Acid, Glycerin, Kaolin, Methylparaben, Polysorbate 80, Propylene Glycol, Polyacrylic Acid, Polyvinylpyrrolidone K90, Propylparaben, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water

  • Usage

    Usage

  • Questions or Comments

    sumifunofficial@gmail.com

  • 158-16

    158-16

  • 158-20

    158-20

  • 158-21

    158-21

  • 158-28

    158-28

  • 158-30

    158-30

  • 158-15

    patch158-15

  • 158-31

    158-31

  • 158-32

    158-32

  • 158-39

    158-39

  • 158-38

    158-38

  • 158-40

    158-40

  • 158-41

    158-41

  • INGREDIENTS AND APPEARANCE
    LIDOCAINE PAIN RELIEF GEL-PATCH 
    lidocaine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83602-158
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    KAOLIN (UNII: 24H4NWX5CO)  
    TARTARIC ACID (UNII: W4888I119H)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83602-158-1515 in 1 BOX10/14/2024
    1NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    2NDC:83602-158-1616 in 1 BOX10/14/2024
    2NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    3NDC:83602-158-2020 in 1 BOX10/14/2024
    3NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    4NDC:83602-158-2121 in 1 BOX10/14/2024
    4NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    5NDC:83602-158-2828 in 1 BOX10/14/2024
    5NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    6NDC:83602-158-3030 in 1 BOX10/14/2024
    6NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    7NDC:83602-158-3131 in 1 BOX10/14/2024
    7NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    8NDC:83602-158-3232 in 1 BOX10/14/2024
    8NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    9NDC:83602-158-3838 in 1 BOX10/14/2024
    9NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    10NDC:83602-158-3939 in 1 BOX10/14/2024
    10NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    11NDC:83602-158-4040 in 1 BOX10/14/2024
    11NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    12NDC:83602-158-4141 in 1 BOX10/14/2024
    12NDC:83602-158-0112 g in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/08/2023
    Labeler - Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (418399704)
    Registrant - Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (418399704)
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