FDA.reportPublic FDA data

FDA label e85b8e2a-d879-4f02-90e2-da0d0c723bbf

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
4fe4e3b0-8a9e-4254-b2c3-88e43caa6d45
SPL ID
e85b8e2a-d879-4f02-90e2-da0d0c723bbf
Version
1
Effective date
2009-11-24
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:31:41

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

WARNINGS For external use only. Do not use in the eyes apply over large areas of the body use on individuals who are allergic or sensitive to iodine use as a first aid antiseptic for longer than 1 week unless directed by a doctor Ask a doctor in case of deep or puncture wounds animal bites serious burns Stop use and ask a doctor if condition persists for more than 72 hours if irritation and redness develop 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.