Otc - Active Ingredient
Salicylic Acid 17%
Bplxkur Wart Remover Liquid
FDA Label NDC 85578-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhengzhou Hangrui Network Technology Co., Ltd. for the product Bplxkur Wart Remover (NDC 85578-008). 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 - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Wart remover
Indications & Usage
for the removal of common warts.
common warts are easily recognized by their rough,"cauliflower-like" appearance.
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Otc - Do Not Use
on irritated skin
on infected or reddened skin
on moles
on birthmarks
on warts with hair growing from them
on genital warts
on warts on the face or mucous membranes
Otc - When Using
avoid contact with eyes
if product gets into eyes, flush with water for 15 minutes
avoid inhaling vapors
Otc - Stop Use
discomfort persists
wart remains after 12 weeks of treatment
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
wash affected area
may soak wart in warm water for 5 minutes
dry area thoroughly
apply a small amount at a time to sufficiently cover each wart
let dry
repeat once daily as needed (until wart is removed) for up to 12 weeks
Inactive Ingredient
Glycerin, Aloe Vera, Chamomile, Menthol, Bisabolol, Polyethylene glycol, Water
Package Label.Principal Display Panel
Label (Label)
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