Mqupin Knee Patch

Manufacturer
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Effective date
2025-05-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:00:35

Label at a glance#

ProductMqupin Knee Patch
Active ingredientCAMPHOR (SYNTHETIC), BORNEOL
Label structure13 sections

Dosage and administration

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

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

temporarily relieves minor pain associated with:

■arthritis

■muscle strains

■sprains

■bruises

■ joint pain

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 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

OTC - STOP USE SECTION

■ 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

OTC - ASK DOCTOR SECTION

children 12 years or younger

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions

OTC - QUESTIONS SECTION

mqupin86@gmail.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83781-002-01Mqupin Knee Patch14 in 1 BOXPATCH143
83781-002-02Mqupin Knee Patch28 in 1 BOXPATCH283
83781-002-03Mqupin Knee Patch42 in 1 BOXPATCH423
83781-002-04Mqupin Knee Patch64 in 1 BOXPATCH643
83781-002-05Mqupin Knee Patch100 in 1 BOXPATCH1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83781-002MQUPIN KNEE PATCH (KNEE PATCH) PATCH [ZHENGZHOU MIAOQI PHARMACEUTICAL TECHNOLOGY CO., LTD]3Current NDC, 5 package rows20250509_09772e4b-8193-3771-e063-6394a90a9516.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83781-00283781-002-01, 83781-002-02, 83781-002-03, 83781-002-04, 83781-002-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mqupin Knee PatchKNEE PATCHZhengzhou Miaoqi Pharmaceutical Technology Co., Ltd09772e4b-8193-3771-e063-6394a90a95162025-05-08WarningsExact identifier
ndc (package): 83781-002-01
ndc (package): 83781-002-05
ndc (package): 83781-002-03
ndc (package): 83781-002-02
ndc (package): 83781-002-04
ndc (product): 83781-002
ndc11 (package): 83781000202
ndc11 (package): 83781000205
ndc11 (package): 83781000203
ndc11 (package): 83781000201
ndc11 (package): 83781000204
spl id: 349c91e3-026f-ba51-e063-6394a90a3fa3
spl set id: 09772e4b-8193-3771-e063-6394a90a9516

Reported adverse events (FAERS/openFDA)#

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