Otc - Active Ingredient
Salicylic Acid
Goodnites Wart Remover Liquid
FDA Label NDC 85578-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhengzhou Hangrui Network Technology Co., Ltd. for the product Goodnites Wart Remover (NDC 85578-001). 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 - when using, 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
For removing common warts and plantar warts.
Warnings
For external use only
Otc - When Using
When using this product, avoid contact witheyes. lf the product gets into your eyes, rinsewith water for 15 minutes. Avoid inhalingfumes. Close the cap tightly and store atroom temperature, away from heat sources
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact aPoison Control Center(1-800-222-1222)right away.
Dosage & Administration
1. Clean and soften the affected
Area with warm water and dry it.
2.Apply the wart remover to each affected areausing the disposable applicator.Apply once in the morning and once in the
3.evening, daily.
Inactive Ingredient
BORNEOL
GLYCERIN
PODOFILOX
POLYETHYLENE GLYCOL, UNSPECIFIED
WATER
Package Label.Principal Display Panel
Label1 (Label1)
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