Otc - Active Ingredient
DL-Camphor 1.2%
L-Menthol 5.7%
Methyl Salicylate 6.3%
Knee Pain Relief Patch
FDA Label NDC 85839-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Finona Information Technology Co., Ltd for the product Knee Pain Relief Patch (NDC 85839-006). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Topical Analgesic
Indications & Usage
For temporary relief of minor aches and pains of muscles and joints associated with:
Arthritis Strainsm Bruisesm Sprains
Warnings
For external use only.
Otc - Do Not Use
If you are allergic to aspirin or salicylates.
With a heating pad.
With, or at the same time as, other external analgesic products
Otc - When Using
Use only as directed
Avoid contact with the eyes, mucous membranes, or rashes
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Clean and dry the affected area.
Remove a patch from the film.
Apply the patch to the affected area for not more than 3 to 4 times a day for 7 days.
You can wear the patch for up to 8 hours per application.
Adults and children 12 years of age and over: Consult a doctor
Inactive Ingredient
Dried Ginger
Cinnamon
Orange Peel
Glycerol
Package Label.Principal Display Panel
Label6 (Label6)
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