FDA.reportPublic FDA data

FDA label 616db97b-6da1-21c0-e053-2991aa0ab688

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
eca6e2ce-bb1e-4954-b384-753cb295c704
SPL ID
616db97b-6da1-21c0-e053-2991aa0ab688
Version
2
Effective date
2017-12-28
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 05:40:34

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 Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use: in the eyes or apply over large areas of the body longer than 1 week unless directed by a doctor on individuals who are sensitive or allergic to iodine Stop use and ask a doctor if: if irritation and redness develop. condition persists more than 72 hours in case of deep or puncture wounds, animal bites or serious burns

Reported adverse events (FAERS/openFDA)#

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