FDA.reportPublic FDA data

FDA label 34007285-999e-6dcc-e063-6294a90a7108

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
26404437-1fa7-f78d-e063-6394a90ad8e4
SPL ID
34007285-999e-6dcc-e063-6294a90a7108
Version
2
Effective date
2025-04-30
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:45:48

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 ■ over large areas of the body ■ if you are allergic to povidone-iodine or any other ingredients in this preparation Ask a doctor before use if you have ■ deep or puncture wounds ■ serious bums ■ animal bites Stop use and ask a doctor if ■ the condition persists or gets worse ■ you need to use this product for more than 1 week 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.