Active Ingredient
Borneol 1.2%
Camphor 1.5%
Mqupin Knee Patch
FDA Label NDC 83781-011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhengzhou Miaoqi Medical Technology Co., Ltd. for the product Mqupin Knee Patch (NDC 83781-011). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, when using, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Use
For sub healthy people with discomfort caused by neck, shoulder,waist and leg.
Warnings
For external use only.
When Using
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
keep out of reach of children
Directions
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
Other Information
store at room temperature, not to exceed 86°F (30°C)
Inactive Ingredients
Mugwort oil, sweet-scented osmanthus oil, eucalyptus oil, cinnamon, dried ginger, suberect, spatholobus stem, magnetic powder, kusnezoff monkshood root, herba speranskiae tuberculatae
Questions
Questions or comments?
Email: [email protected]
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