FDA label 126e27c0-ea60-51bc-e063-6394a90a81e1

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)

SPL set ID: 0fc0970d-06a4-ade9-e063-6394a90ae7ff
SPL ID: 126e27c0-ea60-51bc-e063-6394a90a81e1
Version: 2
Effective date: 2024-02-28
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:33:29

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		126e27c0-ea60-51bc-e063-6394a90a81e1	id
spl set id		0fc0970d-06a4-ade9-e063-6394a90ae7ff	set_id

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 Do not use it on your face..External use only. Pregnant and breastfeeding women should be usedwith caution * Avoid getting the product into your eyes. if it accidentally getsinto theeyes, rinse it off with water immediately..stop using and ask a physician if irritation occurs.Stop use if there is no improvement within d weeks.. keep it away from children.. it is normal for the treated wart to appear red and swollen if thishappens, stop using the product for 3-5 days Once the rednesssubsides, continue to use the product until the wart completely folls off.

Reported adverse events (FAERS/openFDA)#

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