Label: SUMIFUN KNEE RELIEVING PATCH- knee relieving patch patch

  • NDC Code(s): 83781-008-01
  • Packager: Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 6, 2024

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  • Active Ingredient

    Borneol 1.2%
    Camphor 1.5%
    Menthol 1.0%

  • Purpose

    Topical Anaglesic

  • Use

    Temporarily relieves muscle soreness and minor joint pains in the 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

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

  • Stop Use

    ·skin reactions such as redness,swelling,blistering or other discomfort occur
    ·symptoms persist for more than 7 days

  • Ask Doctor

    Children under age of 12

  • Keep Out Of Reach Of Children

    Keep out of reach of children

  • Directions

    ·Clean and dry the affected area.
    ·Peel off the large protective film to reveal a small film on the reddish brown patch.
    ·Partially peel back the protective film and apply the exposed part of the patch to the the site of pain.
    ·Carefully remove remaining film while pressing the patch firmly on the skin.
    ·Remove patch from the skin after at most 8-hour application.

  • Inactive ingredients

    Dried ginger, Saffron, Wormwood, Mugwort oil, Osmanthus flower oil, Eucalyptus leaf oil,Cinnamon

  • Questions

    sumifunofficial@gmail.com

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    SUMIFUN KNEE RELIEVING PATCH 
    knee relieving patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83781-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)1.5 g  in 100 
    BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X) BORNEOL1.2 g  in 100 
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    SAFFRON (UNII: E849G4X5YJ)  
    ARTEMISIA VULGARIS TOP OIL (UNII: 72Q967Y48V)  
    WORMWOOD (UNII: F84709P2XV)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    CINNAMON (UNII: 5S29HWU6QB)  
    GINGER (UNII: C5529G5JPQ)  
    OSMANTHUS FRAGRANS FLOWER (UNII: 4VA0BH57HU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83781-008-0124 in 1 BOX; Type 0: Not a Combination Product01/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/02/2024
    Labeler - Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd (701762807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd701762807label(83781-008) , manufacture(83781-008)
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