Other
Knee Pain Relief Patch
Knee Pain Relief Patch
FDA Label NDC 81484-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anhui Miao De Tang Pharmaceutical Co., Ltd. for the product Knee Pain Relief Patch (NDC 81484-102). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
camphor 3.1%
menthol 6%
methyl salicylate 10%
Otc - Purpose
For the temporary relief of minor aches and pains of muscles and joints associated with.
simple backache.
arthritis.
strains.
bruises.
sprains.
Indications & Usage
Adults and children 2 years of age and older
clean and dry the affected area.
remove the patch from the release liner.
apply to affected area not more than 3 to 4 times daily.
Warnings
For external use only
Otc - Do Not Use
Children under 2 years of age
do not use, consult a doctor
Otc - When Using
use only as directed.
avoid contact with the eyes.
do not apply to wounds or damaged skin.
do not bandage tightly.
Otc - Stop Use
if condition worsens.
if symptoms persist for more than 7 days.
if symptoms clear up and occur again within a few days.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Dosage & Administration
apply to affected area not more than 3 to 4 times daily
Storage And Handling
avoid storing in direct sunlight
protect from excessive moisture
Inactive Ingredient
eucalyptus, peppermint, thyme, wintergreen
Package Label.Principal Display Panel
Label (Label 2)
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