VERUCIDE WART REMOVER Kit

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
VERUCIDE WART REMOVER Kit
Generic name
WART REMOVER
Manufacturer
Blaine Labs Inc.
Product type
HUMAN OTC DRUG
SPL set ID
017f3ca2-6dba-4db5-b559-8ce0f2709772
SPL ID
8d1b445c-d868-4bc9-855a-785d3b33112e
Version
3
Effective date
2025-01-02
Source export date
2026-10-30
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:27:04

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 - For external use only (for step 1 & 2) Extremely flammable. Keep away from fire or flames

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.