FDA.reportPublic FDA data

FDA label 2a431b1f-e60c-214d-e054-00144ff8d46c

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
825f6f3d-3b29-4fad-8bde-79b19ccf2370
SPL ID
2a431b1f-e60c-214d-e054-00144ff8d46c
Version
2
Effective date
2016-01-26
Source export date
2026-08-01
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/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:17:01

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 if you are allergic to iodine or any of the other ingredients in the product When using this product prolonged exposure to wet solution may cause irritation, or rarely, severe skin reactions in pre-operative prepping, avoid "pooling" beneath the patient Stop use and ask a doctor if irritation and redness develop if condition persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.