Otc - Active Ingredient
Salicylic acid 40%
Wart Remover Patches Patch
FDA Label NDC 87579-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Chuanglian Zhida Trading Co., Ltd for the product Wart Remover Patches (NDC 87579-003). 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 - keep out of reach of children, dosage & administration, inactive ingredient, 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
Helps alleviate local skin discomfort caused by warts, keratinization,skin thickening, or roughness.
Warnings
For external use only.
Otc - Do Not Use
On inflamed, ulcerated, or damaged skin.
On genital warts and warts on the face.
On mucous membranes
Not for use by pregnant or breastfeeding women.
Otc - Keep Out Of Reach Of Children
If swallowed,get medical help or contact a Poison Control Centerright away.
Dosage & Administration
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 tofit wart Carefully apply medicated plaster,
repeat procedure every 48 hours as needed (until wart is removed) for up to 12 week.
Small warts (1-3 mm) typically shed within 30 days with over 90% success rate;medium warts (3-5 mm) gradually dry and fall off within 60 days,with no recurrence reported.
Inactive Ingredient
Portulaca Oleracea Extract
Lithospermum erythrorhizon root
Mume Fructus
Rhus Chinensis Gall
Borneol
Camphor (Natural)
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