Label: MQFORU PAIN PATCH- pain patch patch

  • NDC Code(s): 83781-010-01, 83781-010-02, 83781-010-03, 83781-010-04, view more
    83781-010-05, 83781-010-06, 83781-010-07
  • Packager: Zhengzhou Miaoqi Medical Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 12, 2024

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

  • Active Ingredient

    Menthol 2.0%

    Borneol 1.2%

    Camphor 1.5%

  • Purpose

    Topical Analgesic

  • Use

    for sub healthy people with discomfort caused by neck, shoulder,waist and leg pain.

  • Warnings

    For external use only.

  • Do not use

    When using this product

    ■ 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

  • When Using

    When using this product

    ■ 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

    Stop use and ask doctor if:

    ■ 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

    Stop use and ask doctor if:

    ■ 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

  • Keep Out Of Reach Of Children

    ■ Keep out of reach of children

  • 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
    children 12 years or younger: ask a doctor

  • Other information

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

  • Inactive ingredients

    Radix Angelicae Pubescentis, Drynaria Rhizome, Myrrh, Frankincense, Elderberry, Safflower, Angelicae, and Trachlospermi Caulis Et Folium

  • Questions

    Questions or comments?

    Email: mqforu86@gmail.com

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    MQFORU PAIN PATCH 
    pain patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83781-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 g  in 100 
    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
    ANGELICA BISERRATA WHOLE (UNII: IAA753UT7B)  
    MYRRH (UNII: JC71GJ1F3L)  
    ANGELICIN (UNII: CZZ080D7BD)  
    TRACHELOSPERMUM JASMINOIDES STEM (UNII: 7YF691N2XM)  
    EUROPEAN ELDERBERRY (UNII: BQY1UBX046)  
    DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)  
    SAFFLOWER (UNII: 4VBL71TY4Y)  
    FRANKINCENSE (UNII: R9XLF1R1WM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83781-010-0110 in 1 BOX; Type 0: Not a Combination Product08/13/2024
    2NDC:83781-010-0220 in 1 BOX; Type 0: Not a Combination Product08/13/2024
    3NDC:83781-010-0330 in 1 BOX; Type 0: Not a Combination Product08/13/2024
    4NDC:83781-010-0440 in 1 BOX; Type 1: Convenience Kit of Co-Package08/13/2024
    5NDC:83781-010-0550 in 1 BOX; Type 0: Not a Combination Product08/13/2024
    6NDC:83781-010-0660 in 1 BOX; Type 0: Not a Combination Product08/13/2024
    7NDC:83781-010-07100 in 1 BOX; Type 0: Not a Combination Product08/13/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/13/2024
    Labeler - Zhengzhou Miaoqi Medical Technology Co., Ltd. (701762807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhengzhou Miaoqi Medical Technology Co., Ltd.701762807manufacture(83781-010) , label(83781-010)