Otc - Active Ingredient
Salicylic acid 12%
Wart Remover Patches Patch
FDA Label NDC 85839-009
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 Wart Remover Patches (NDC 85839-009). 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
Wart Remover
Indications & Usage
For the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-ike' appearance of the sruface
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 - When Using
Ask a doctor before use if you have diabetes poor blood circulatio
Otc - Keep Out Of Reach Of Children
If swallowed, get medica help or contact a Poison Control Center right away
Dosage & Administration
wash affected area may soak wart in warm water for 5 minutes dryarea thoroughlyremove bandage strips by peeling backing offif necessary, cut medicated patch to fit wartcarefully apply medicated plasterrepeat procedure every 48 hours as needed(until wart is removed)for up to 12 week
Inactive Ingredient
hard paraffin
lanolin
phenol
borneol
crocus sativus L
gleditsia sinensis Lam
Package Label.Principal Display Panel
Label1 (Label1)
* Please review the disclaimer below.
