FDA label 4308a97e-2692-211c-e063-6294a90a033c

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
c6190453-4385-4be5-b4b9-4637b4e84845
SPL ID
4308a97e-2692-211c-e063-6294a90a033c
Version
6
Effective date
2025-11-07
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:05:38

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 if allergic to iodine or in the eyes Ask a doctor before use if injuries are deep wounds, puncture wounds, or serious burns Stop use and ask a doctor if infection occurs or if redness, irritation, swelling or pain persists or increases. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately. Avoid excessive heat. Store at room temperature.

Reported adverse events (FAERS/openFDA)#

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