Active Ingredient
Ginger
Mugwort Pain Relief Patch
FDA Label NDC 84732-092
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguan Haiyi Technology Co.,ltd. for the product Mugwort Pain Relief Patch (NDC 84732-092). 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, inactive ingredient, purpose section, warning, stop use, not use, out of children, how to use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Wormwood,Radix aconti.
Purpose Section
Relieve joint, lumbar, cervical, knee, and leg pain
Warning
1.For external use only.
2.lf any allergy or discomfort occurs during use, please stopusing the product.
3.Keep away from children and pets.
Stop Use
lf any allergy or discomfort occurs during use, please stop using the product.
Not Use
Not suitable for use by children, pregnantor breast feeding people.
Out Of Children
KEEP THE PRODUCT OUT OF REACH OF CHILDREN to
How To Use
Attached directly to body parts, it is safe to use and has no side effects.
Dosage
take an appropriateamount,Use 2-3 times a week
Package Label.Principal Display Panel
Label (59b5bee659234dc0845fcc65661775f4)
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