Otc - Active Ingredient
Salicylic Acid
Wart Remover Liquid
FDA Label NDC 88064-123
8 label sections · Submitted to the FDA by Shenzhen Baifanghui Technology Co., Ltd · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Baifanghui Technology Co., Ltd for the product Wart Remover (NDC 88064-123). 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, indications & usage, warnings, 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
Wart remover
Otc - Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center immediately
Indications & Usage
Uses for the removal of common warts for the removal of plantar warts
Directions
wash affected area; apply a thin layer; allow to dry; repeat once or twice daily; continue use up to 12 weeks
Warnings
For external use only.
Avoid contact with eyes and healthy skin.
Keep out of reach of children.
Flammable.
Keep away from heat and fire.
Dosage & Administration
Repeat once or twice daily; continue use up to 12 weeks
Inactive Ingredient
Alcohol, Lactic Acid, Water
Package Label.Principal Display Panel
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