FDA.reportPublic FDA data

FDA label f6cd206d-c5df-7924-e053-6294a90a7530

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
300c1c06-4dcd-41f9-bcb9-dec1308e08d6
SPL ID
f6cd206d-c5df-7924-e053-6294a90a7530
Version
6
Effective date
2023-03-13
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:49:37

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, nose or mouth on individuals who are allergic or sensitive to iodine over large areas of the body as a first aid antiseptic longer than one week unless directed by a doctor Discontinue use if irritation and redness develop. If condition persist for more than 72 hours or gets worse, consult a healthcare provider Consult a healthcare provier in case of Deep or puncture wounds animal bites serious burns if you are pregnant Avoid pooling

Reported adverse events (FAERS/openFDA)#

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