Home DailyMed e3b4c4a2-e91c-4c39-e053-2995a90aefe8 Medicated Wart Remover Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Premier Brands of America, Inc.
Effective date 2024-10-14
Label type HUMAN OTC DRUG LABEL
Version 4
Source legacy-cache
Hydrated at 2026-08-01 20:52:38 Label at a glance# Product Medicated Wart Remover
Active ingredient SALICYLIC ACID
Label structure 9 sections
Dosage and administration wash affected area: may soak wart in warm water for 5 minutes dry area thoroughly if necessary, cut medicated patch directly over wart cover patch with pad to conceal area repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56104-260 MEDICATED WART REMOVER (SALICYLIC ACID) PATCH [PREMIER BRANDS OF AMERICA, INC.] 4 Legacy NDC 20241016_e3b4c4a2-e91c-4c39-e053-2995a90aefe8.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 5 matching rows.
Medicated Wart Remover Salicylic acid POLYVINYL ALCOHOL, UNSPECIFIED HIGH DENSITY POLYETHYLENE VINYL ACETATE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 4 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.