Active Ingredient
Borneol 15.0%
Tendon Sheath Patch
FDA Label NDC 83675-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Hanhai Trading Co., Ltd for the product Tendon Sheath Patch (NDC 83675-006). 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, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Relief Joint Pain
Use
Tendon Sheath Patch to help relief joint pain
Warnings
For external use only. Do not take it internally.
Keep Out Of Reach Of Children
Prohibited for those with damaged skin.
Do Not Use
Product shall not be eat
When Using
Do not stick around eyes and mouth,This product cannot replace drugs.
Stop Use
In case of adverse reactions, please stop using this product.If the symptoms.
Ask Doctor
ask doctor in case of adverse reactions
Keep Oot Of Reach Of Children
Keep Out Of Reach Of Children
Directions
Take one piece of this product when needed, remove the waxpaper,
stick to the desired area and press the surrounding, replace it every 8-12 hours.
Children should be used under adult supervision.
Other Information
Store the product in a cool, dry and well-ventilated place
Avoid direct sunlight
Inactive Ingredients
Processed Pinellia,
Radix Aconiti PreparataRadix Aconiti Kusnezoffi PreparaHerba Lycopi,
Radix Angelicae Sinensis,
Flos Carthami,
Scorpio,
centipede.
GroundBeetle,
Zanthoxvlum huskl.
Menthol.
Centipede Hot melt alue
Principal Display Panel
01 (51d8039f1bff657895921785b700621)
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