Label: TIGER PAIN RELIEF PATCH patch

  • NDC Code(s): 83675-012-01
  • Packager: Guangzhou Hanhai Trading Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 20, 2023

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  • Active Ingredient

    Menthol 19.0%

  • Purpose

    Pain Relief

  • Use

    Temporarily relieves muscle soreness and minor joints pain related to arthritis, backache, strains, sprains

  • Warnings

    For external use only. Do not take it internally.

    Keep Out Of Reach Of Children
    Sensitive Skin

  • Do not use

    Product shall not be eat

  • When Using

    Use only as directedAvoid contacting with eyes or mucous membranesDo not apply to wounds or damaged skinDo not use with other ointments, creams, sprays, or linimentsDo not bandage or use with heating pad or devictStore in a cool dry place away from direct sunlight

  • Stop Use

    In case of adverse reactions, please stop using this product.If the symptoms.

  • Ask Doctor

    ask doctor in case of Sensitive Skin

  • Keep Oot Of Reach Of Children

    Keep Out Of Reach Of Children

  • Directions

    Take one piece of this product when needed, remove the waxpaper,

    stick to the desired area and press the surrounding, replace it every 8 hours.

    Children should be used under adult supervision.

  • Other information

    Store the product in a cool, dry and well-ventilated place

    Avoid direct sunlight

  • Inactive ingredients

    Far-infrared Nano Ceramic Powder,

    Medical Adhesive Paste,

    Backing

    Silicone Oil Paper

  • PRINCIPAL DISPLAY PANEL

    01

  • INGREDIENTS AND APPEARANCE
    TIGER PAIN RELIEF PATCH 
    tiger pain relief patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83675-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL19 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    BACKHOUSIA MYRTIFOLIA WHOLE (UNII: M5B93S0VJK)  
    DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 1000000 PA.S) (UNII: 83D19O7250)  
    IVERMECTIN (UNII: 8883YP2R6D)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83675-012-018 in 1 BAG; Type 0: Not a Combination Product09/19/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34809/19/2023
    Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Hanhai Trading Co., Ltd419707381label(83675-012) , manufacture(83675-012)
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