FDA.reportPublic FDA data

FDA label c1baa608-27fa-4efe-b0a4-b4c1c6c7489e

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
4f8a29aa-8f0f-4c62-8552-54b8bba9a613
SPL ID
c1baa608-27fa-4efe-b0a4-b4c1c6c7489e
Version
1
Effective date
2017-05-31
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 01:25:54

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 if allergic to iodine in the eyes Ask a doctor before use if injuries are deep wounds puncture wounds serious burns Stop use and ask a doctor if redness, irritation, swelling or pain persists or increases infection occurs For external use only Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately. Avoid pooling beneath the patient. Prolonged exposure to wet solution may cause skin irritation.

Reported adverse events (FAERS/openFDA)#

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