FDA.reportPublic FDA data

FDA label f42b2912-2498-7619-e053-2a95a90ae1ba

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
64c46ae9-3b3c-4b1c-a6be-c8aea17f313b
SPL ID
f42b2912-2498-7619-e053-2a95a90ae1ba
Version
2
Effective date
2023-02-08
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:29

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 burns • 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 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.