Otc - Active Ingredient
Salicylic acid 8% w/w
Zrizl Wart Remover Liquid
FDA Label NDC 85593-015
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 Chuanma International Trading Co.,ltd. for the product Zrizl Wart Remover (NDC 85593-015). 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, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, indications & usage, 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
Uses For The removai ol s corns, calluses, piantar warts, filat warts, comman warts (less than 5 mmin stze)
Warnings
Warnings o For exernal use only ，Keep away fromheat or flame
Otc - Keep Out Of Reach Of Children
Keep out of reach ofchildren, lfswallowed, get medical help or contact a Poison controt center right a-way
Dosage & Administration
Wash the affected area ， Soak the.wartsin warm water for 5 minutes aind dryit thoroughly Apply one drop at a time with the applicator to cov.er the warts completely o Allow to dry, use self adhesive cushloning pads to cover the warts if deslred@Repeat this pracess once or twice dally as neededfor up to 12 weeks, until the warts is removed (Nte.For external use, and can not be applied to healthy skin)
Inactive Ingredient
ALCOHOL
SOPHORA FLAVESCENS ROOT
LITHOSPERMUM INCISUM WHOLEANGELICA DAHURICA VAR. FORMOSANA WHOLEBRUCEA JAVANICA WHOLE
Indications & Usage
keep out of eyes, ear ;and mouth if product gets in eyes, flush with waterfor 15 minutes
Package Label.Principal Display Panel
Labeling (85593 015 01)
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