FDA label 75ffc2d3-b014-4e28-a7ae-76b61646f8e1

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
80ebc348-b7c9-4d99-8c3b-2a79fef08902
SPL ID
75ffc2d3-b014-4e28-a7ae-76b61646f8e1
Version
1
Effective date
2012-05-21
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:40:41

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

FOR EXTERNAL USE ONLY DO NOT Use in the eyes Use on individuals who are allergic of sensitive to iodine Apply over large areas of the body Discontinue use and ask a doctor If condition persist or gets worse For use longer than 1 week Ask a doctor in case of Deep or punctured wounds Animal bites Serious burns

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.