Otc - Active Ingredient
SALICYLIC ACID
Sottsunfeli Wart Remover Liquid
FDA Label NDC 85136-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Henan Toudaorong Biotechnology Co., Ltd. for the product Sottsunfeli Wart Remover (NDC 85136-010). 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, otc - keep out of reach of children, warnings, indications & usage, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
for the removal of common and plantar warts
Otc - Keep Out Of Reach Of Children
Keep out of reach of chlldren
Warnings
For external use only. Flammable.
Keep away from fire and flame.
Indications & Usage
Wash the affected area.
May soak wart in warm water for 5 minutes.
Dry area thoroughly.
Use a brush to apply a sufficient amount to cover each wart. Let it dry.
Repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.
Dosage & Administration
Wash the affected area.
May soak wart in warm water for 5 minutes.
Inactive Ingredient
BORNEOL
POLYETHYLENE GLYCOL, UNSPECIFIED
WATER
GLYCERIN
PODOFILOX
Package Label.Principal Display Panel
Labeling (85136 010 01)
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