Drugplain

Sumifun Knee Relieving Patch 1.2 g/1001

Knee Relieving Patch · PATCH · Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd

No Recall History
Plain English

Sumifun Knee Relieving Patch is a patch containing knee relieving patch at 1.2 g/1001, taken topical. Manufactured by Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd.

Key Facts

Brand Name
Sumifun Knee Relieving Patch
Generic Name
Knee Relieving Patch
NDC Code (Product)
83781-008
Manufacturer
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Strength
1.2 g/1001
Dosage Form
PATCH
Route
TOPICAL
Marketing Status
Application #
M017
Marketing Start
01/02/2024

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

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

Dosage & Administration

Directions ·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.

Warnings

Warnings For external use only.

Frequently Asked Questions

What is Sumifun Knee Relieving Patch used for?

Sumifun Knee Relieving Patch contains Knee Relieving Patch. It is a patch taken topical. Consult your doctor for specific uses.

Is Sumifun Knee Relieving Patch a controlled substance?

Sumifun Knee Relieving Patch is not classified as a controlled substance by the DEA.

What is the generic name for Sumifun Knee Relieving Patch?

The generic name for Sumifun Knee Relieving Patch is Knee Relieving Patch. There are no other listed brand versions of Knee Relieving Patch.

What is the NDC code for Sumifun Knee Relieving Patch 1.2 g/1001?

The NDC (National Drug Code) for Sumifun Knee Relieving Patch 1.2 g/1001 is 83781-008, listed by Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd.

Product NDC

83781-008

Package NDC

83781-008-01

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)