FDA.reportPublic FDA data

FDA label 9ef84712-e6fc-4a27-b9d8-b4e926b8256e

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
8d8a21d3-7d8b-4174-8c21-736cf3d3d869
SPL ID
9ef84712-e6fc-4a27-b9d8-b4e926b8256e
Version
2
Effective date
2014-05-26
Source export date
2026-08-01
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5a565ce64c898c83223b815b9579cd46fb0c6d54977c3cace2133e40124f7fbb/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:08:43

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. For External use only. Ask a doctor before use if injuries are --Deep or puncture wounds --serious bums stop use ask a doctor if --reness ,irritation ,swelling or pain persists or increases --infection occurs Do not use in eyes Avoid "pooling "benesth patient.Prolonged exposure to wet solution may cause skin irrtation. Keep out of reach of children. Keep out of reach of children.in case of axxidental ingestion,seek professional assistance or consult a poison control center immediately.