Active Ingredient
Salicylic acid 40%
Txl Active Wart Remover Pads
FDA Label NDC 83124-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kairos Trading Inc for the product Txl Active Wart Remover Pads (NDC 83124-002). 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, keep oot of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Wart Remover
Use
For the removal of common warts. The common wart is easily recognized by the rough ‘cauliflower-like’ appearance of the surface.
Warnings
For external use only.
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 from them
on mucous membranes
When Using
Ask a doctor before use if you have
diabetes poor blood circulatio
Keep Oot Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
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
Other Information
Store between 59° and 86°F (15° and 30°C).
Inactive Ingredients
hard paraffin, lanolin, phenol
Questions
1-914-875-2018
Package Label
83124-002-01
83124-002-01 (Pack)
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