MQUPIN Knee Patch

Manufacturer: Zhengzhou Miaoqi Medical Technology Co., Ltd.
Effective date: 2025-06-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:02:53

Label at a glance#

ProductMQUPIN Knee Patch

Active ingredientCAMPHOR (SYNTHETIC), BORNEOL

Label structure11 sections

Dosage and administration

adults and children over 12 years: After cleaning and drying the skin, peel off the protective liner of the patch and apply one patch to each knee once daily. children 12 years or younger: ask a doctor

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Borneol 1.2%
Camphor 1.5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When Using

OTC - WHEN USING SECTION

use only as directed
do not bandage tighty or use with a heating pad
avoid contact with eves 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

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mugwort oil, sweet-scented osmanthus oil, eucalyptus oil, cinnamon, dried ginger, suberect, spatholobus stem, magnetic powder, kusnezoff monkshood root, herba speranskiae tuberculatae

Questions

OTC - QUESTIONS SECTION

Questions or comments?

Email: mqupin86@gmail.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
83781-011-01	MQUPIN Knee Patch	24 in 1 BOX	PATCH	24	1
83781-011-02	MQUPIN Knee Patch	36 in 1 BOX	PATCH	36	1
83781-011-03	MQUPIN Knee Patch	60 in 1 BOX	PATCH	60	1
83781-011-04	MQUPIN Knee Patch	100 in 1 BOX	PATCH	100	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

MQUPIN Knee Patch
Knee Patch
ACONITUM NAPELLUS ROOT
SPATHOLOBUS SUBERECTUS WHOLE
CAMPHOR (SYNTHETIC)
GINGER
BORNEOL
CINNAMON
FERROSOFERRIC OXIDE
ACONITUM KUSNEZOFFII LEAF
ARTEMISIA VULGARIS OIL
EUCALYPTUS OIL
3,3-DIMETHYLCYCLOHEXYL METHYL KETONE
SPATHOLOBUS SUBERECTUS STEM
3-HYDROXYTYROSOL 3-O-GLUCOSIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83781-011	83781-011-01, 83781-011-02, 83781-011-03, 83781-011-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ACONITUM NAPELLUS ROOT	KPD2N7348X	IACT
SPATHOLOBUS SUBERECTUS WHOLE	J4FRL97E6E	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
GINGER	C5529G5JPQ	IACT
BORNEOL	M89NIB437X	ACTIB
CINNAMON	5S29HWU6QB	IACT
FERROSOFERRIC OXIDE	XM0M87F357	IACT
ACONITUM KUSNEZOFFII LEAF	SXZ33Q1M29	IACT
ARTEMISIA VULGARIS OIL	72Q967Y48V	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
3,3-DIMETHYLCYCLOHEXYL METHYL KETONE	MH1R8F7762	IACT
SPATHOLOBUS SUBERECTUS STEM	N51VZ363BA	IACT
3-HYDROXYTYROSOL 3-O-GLUCOSIDE	J88XB1FJ39	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MQUPIN Knee Patch	KNEE PATCH	Zhengzhou Miaoqi Medical Technology Co., Ltd.	37438a70-dab7-ecb5-e063-6394a90afefb	2025-06-10	Warnings	Exact identifier ndc (package): 83781-011-04 ndc (package): 83781-011-03 ndc (package): 83781-011-01 ndc (package): 83781-011-02 ndc (product): 83781-011 ndc11 (package): 83781001104 ndc11 (package): 83781001102 ndc11 (package): 83781001103 ndc11 (package): 83781001101 spl id: 37438a70-dab8-ecb5-e063-6394a90afefb spl set id: 37438a70-dab7-ecb5-e063-6394a90afefb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.