Home FDA labels 437490e6-39c5-a79c-e063-6394a90ac0f9 WART REMOVER openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name WART REMOVER
Generic name WART REMOVER
Manufacturer Shenzhen Mengyue Technology Co., Ltd.
Product type HUMAN OTC DRUG
SPL set ID 437490e6-39c4-a79c-e063-6394a90ac0f9
SPL ID 437490e6-39c5-a79c-e063-6394a90ac0f9
Version 1
Effective date 2025-11-13
Source export date 2026-11-06
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 07:25:15 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 11 matching rows.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS · The liquid can get easily volatilized & crystallized, tighten the cap after use. · Avoid long-term contact with air while using. · For external use only, don't contact with eyes or swallow.Children should use it under the supervision of adults.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.