FDA label 36580895-2731-1682-e063-6394a90ae34b

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: 123fe940-22d6-1658-e063-6294a90afca5
SPL ID: 36580895-2731-1682-e063-6394a90ae34b
Version: 3
Effective date: 2025-05-30
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:53:48

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		36580895-2731-1682-e063-6394a90ae34b	id
spl set id		123fe940-22d6-1658-e063-6294a90afca5	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.