SALZIX 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
SALZIX WART REMOVER
Generic name
SALICYLIC ACID
Manufacturer
Toprail Chp Llc
Product type
HUMAN OTC DRUG
SPL set ID
69864363-ecd7-4b08-ba9e-ecd1a3e95f37
SPL ID
b71df063-c5d7-4a4f-a638-f004158631e4
Version
1
Effective date
2025-03-20
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:09:58
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 For external use only. Flammable • keep away from fire or flame Do not use • if you are diabetic of if you have poor blood circulation • on genital warts or warts on the face or mucous membrane • on moles, birthmarks or warts with hair growing from them • on irritated skin or on any area that is infected or reddened When using this product • If product gets into the eye, flush with water for 15 minutes • avoid inhaling vapors • cap bottle tightly and store at room temperature away from heat Stop use and ask a doctor if discomfort persists. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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