Active Ingredient
Menthol 19.0%
Menthol Patch
FDA Label NDC 83675-010
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 Menthol Patch (NDC 83675-010). 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
Pain Relief
Use
Temporarily relieves muscle soreness and minor joints pain related to arthritis, backache, strains, sprains
Warnings
For external use only. Do not take it internally.
Keep Out Of Reach Of Children
Sensitive Skin
Do Not Use
Product shall not be eat
When Using
Use only as directedAvoid contacting with eyes or mucous membranesDo not apply to wounds or damaged skinDo not use with other ointments, creams, sprays, or linimentsDo not bandage or use with heating pad or devictStore in a cool dry place away from direct sunlight
Stop Use
In case of adverse reactions, please stop using this product.If the symptoms.
Ask Doctor
ask doctor in case of Sensitive Skin
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 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
Far-infrared Nano Ceramic Powder,
Medical Adhesive Paste,
Backing
Silicone Oil Paper
Principal Display Panel
01 (Ac5c8e33e8f3da4f37df9be953493b3)
* Please review the disclaimer below.
