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
SALICYLIC ACID
Manufacturer
Guangzhou Hechuang Commercial Service Co.,Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
59df0688-5d06-1da4-e063-6394a90a799b
SPL ID
59df069d-8078-76e9-e063-6294a90a7512
Version
1
Effective date
2026-08-25
Source export date
2026-10-30
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:20:58
Harmonized routes table
Harmonized routes
TOPICAL

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 Warnings • For external use only. • Keep away from fire or flame. Do not use • on irritated, infected, or reddened skin • on moles, birthmarks, warts with hair growing from them,or genital warts • on warts on the face or mucous membranes • if you have diabetes or poor blood circulation When using this product • avoid contact with eyes • if product gets into the eyes, flush with water for 15 minutes • avoid contact with surrounding healthy skin • avoid inhaling vapors

Reported adverse events (FAERS/openFDA)#

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