Sumifun Knee Relieving Patch

Manufacturer
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Effective date
2024-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:06:52

Label at a glance#

ProductSumifun Knee Relieving Patch
Active ingredientCAMPHOR (SYNTHETIC), BORNEOL, MENTHOL
Label structure13 sections

Dosage and administration

·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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Borneol 1.2%
Camphor 1.5%
Menthol 1.0%

Purpose

OTC - PURPOSE SECTION

Topical Anaglesic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves muscle soreness and minor joint pains in the knees, back,neck,hips,shoulders,elbows.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

·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

OTC - WHEN USING SECTION

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

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

Children under age of 12

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

·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

INACTIVE INGREDIENT SECTION

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

Questions

OTC - QUESTIONS SECTION

sumifunofficial@gmail.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83781-008-01Sumifun Knee Relieving Patch24 in 1 BOXPATCH241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83781-008SUMIFUN KNEE RELIEVING PATCH (KNEE RELIEVING PATCH) PATCH [ZHENGZHOU MIAOQI PHARMACEUTICAL TECHNOLOGY CO., LTD]1Current NDC, 1 package rows20240110_0e7e73ec-ab33-9235-e063-6394a90ad950.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83781-00883781-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Sumifun Knee Relieving PatchKNEE RELIEVING PATCHZhengzhou Miaoqi Pharmaceutical Technology Co., Ltd0e7e73ec-ab33-9235-e063-6394a90ad9502024-01-06WarningsExact identifier
ndc (package): 83781-008-01
ndc (product): 83781-008
ndc11 (package): 83781000801
spl id: 0e7e7a45-0a9d-7430-e063-6294a90a894f
spl set id: 0e7e73ec-ab33-9235-e063-6394a90ad950

Reported adverse events (FAERS/openFDA)#

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