Label: MQUPIN KNEE PATCH- knee patch patch

  • NDC Code(s): 83781-002-01, 83781-002-02
  • Packager: Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Borneol 1.2%
    Camphor 1.5%

  • Purpose

    Topical Analgesic

  • Use

    temporarily relieves minor pain associated with:

    ■arthritis

    ■muscle strains

    ■sprains

    ■bruises

    ■ joint pain

  • Warnings

    For external use only.

  • When Using

    ■ use only as directed

    ■ do not bandage tighty or use with a heating pad

    ■ avoid contact with eyes and mucous membranes

    ■ do not apply to wounds or damaged, broken or imitated skin

    ■ do not use at the same time as other topical analgesics

  • Stop Use

    ■ rash, itching or excessive skin irritation develops

    ■ condition worsens

    ■ symptoms persist for more than 7 days

    ■ symptoms clear up and occur again within a few days If pregnant or breastfeeding, 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

  • Ask Doctor

    children 12 years or younger

  • Keep Out Of Reach Of Children

    Keep Out Of Reach Of Children

  • Directions

  • Directions

    adults and children over 12 years:

    ■clean and dry the affected area

    ■remove backing from patch and apply patch to affected area

    ■use 1 patch per knee for 8 to 12 hours, once per day

  • Other information

    store at room temperature, not to exceed 86°F (30°C)

  • Inactive ingredients

    Dried ginger, saffron, Wormwood, mugwort oil, osmanthus flower oil, eucalyptus leaf oil, cinnamon.

  • Questions

    mqupin86@gmail.com

  • PRINCIPAL DISPLAY PANEL

    01

  • INGREDIENTS AND APPEARANCE
    MQUPIN KNEE PATCH 
    knee patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83781-002
    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 
    Inactive Ingredients
    Ingredient NameStrength
    ARTEMISIA VULGARIS TOP OIL (UNII: 72Q967Y48V)  
    CINNAMON (UNII: 5S29HWU6QB)  
    WORMWOOD (UNII: F84709P2XV)  
    OSMANTHUS FRAGRANS FLOWER (UNII: 4VA0BH57HU)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    SAFFRON (UNII: E849G4X5YJ)  
    GINGER (UNII: C5529G5JPQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83781-002-0114 in 1 BOX; Type 0: Not a Combination Product11/05/2023
    2NDC:83781-002-0228 in 1 BOX; Type 0: Not a Combination Product11/05/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/05/2023
    Labeler - Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd (701762807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd701762807label(83781-002) , manufacture(83781-002)