FDA.reportPublic FDA data

FDA label 021d76b8-2021-43e7-be7c-cf9135742bcb

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
67fa81ec-b022-40c5-8f62-5286b145356a
SPL ID
021d76b8-2021-43e7-be7c-cf9135742bcb
Version
2
Effective date
2010-03-22
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:16

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. Do not use in the eyes apply over large areas of the body use on individuals who are allergic or sensitive to iodine use as a first aid antiseptic for longer than 1 week unless directed by a doctor Ask a doctor in case of deep or puncture wounds animal bites serious burns Stop use and ask a doctor if condition persists for more than 72 hours if irritation and redness develop 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.