Otc - Active Ingredient
Active ingredients
2%Menth0l...............
Purpose
Topical Analgesic
Mugwort Patch (knee Use) Patch
FDA Label NDC 87267-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiyangyuan Life Sciences (hong Kong) Co., Limited for the product Mugwort Patch (knee Use) (NDC 87267-004). 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 otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, indications & usage, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses
For relief of aches, pains and inflammations of muscles and joints associated with:
Knee pain
Knee osteoarthritis Meniscus injury I
MPatellar tendinitis
Synovitis
Ligament injury
Warnings
WaringsFor external use only.
Otc - Keep Out Of Reach Of Children
Place it out of reach of children;
Indications & Usage
When using this product
It is forbidden to use around the eyes,mucous membranes and skin ulcers or infected areas;If there are abnormal conditions such as rashes and itching after use,please stop using it immediately;It is forbidden to use for infants and young children;
Continuous use of the same area may damage the skin.
Dosage & Administration
Directions
1.Wipe off the oil and sweat on the skin surface;
2. Remove the anti-sticking paper on the surface and stick it on the target area;
3.Each patch can be used for 8 hours.
Inactive Ingredient
Inactive ingredients
Wormwood oil,Borneol,Camphor,Capsicum Oleoresin,Rosin
Package Label.Principal Display Panel
Labeling (87267 004 01)
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