Otc - Active Ingredient
salicylic acid 1%
Wart Remover Patch
FDA Label NDC 84023-110
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 Yangan Technology Co., Ltd. for the product Wart Remover Patch (NDC 84023-110). 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 - do not use, otc - keep out of reach of children, otc - when using, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Wart Remover
Warnings
For external use only.
Otc - Do Not Use
on irritated, infected or reddened skin
on genital warts and warts on the face
on moles, birthmarks and warts with hair growing form them
on mucous membranes
Otc - Keep Out Of Reach Of Children
keep out of reach of children
If swallowed, get medica help or contact a Poison Control Center right way
Otc - When Using
when using
Ask a doctor before use if you have diabetes poor blood circulatio
Dosage & Administration
One patch per day, each patch contains 1 mg of tolnaftate.
Other Safety Information
Store between 59° and 86'F (15° and 30° C)
Inactive Ingredient
hard paraffin, lanolin, phenol
Indications & Usage
DIRECTIONS
wash affected area:may soak wart in warm water for 5 minutes
dry area thoroughly
remove bandage strips by peeling backing off
if necessary, cut medicated patch to fit wart
carefully apply medicated plaster
repeat procedure every 48 hours as needed(until wart is removed)
for up to 12 week
* Please review the disclaimer below.
