FDA.reportPublic FDA data

FDA label a8b5be70-d3d0-4858-80fd-e73f58072cac

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
d4839bfa-4e7a-0431-a7b8-8a34360ae30a
SPL ID
a8b5be70-d3d0-4858-80fd-e73f58072cac
Version
6
Effective date
2023-08-01
Source export date
2026-11-06
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/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:58:55

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 externaluse only Do not use in the eyes over large areas of the body if you are allergic to povidone-iodine or any other ingredientsin this preparation Ask a doctor beforeuse if you have deep or puncture wounds serious burns animal bites Stop use and aska doctor if the condition persists or gets worse you need to use this product for more than 1 week Keep out of reach of children. If swallowed, getmedical 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.