FDA label 0ea3bfb3-7e20-5267-e063-6294a90a1a99

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
83aeea44-a693-337e-e053-2a91aa0a533d
SPL ID
0ea3bfb3-7e20-5267-e063-6294a90a1a99
Version
9
Effective date
2024-01-10
Source export date
2026-10-22
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-22/63b92dadbf6487b575e111b437d26dfb89c1d6401bf1507c742074f4503ba64d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run
20261023T001338Z
Imported at
2026-10-23 00:19:35

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 2 of 2 · 5 matching rows.

warnings

PVP Warnings For external use only Do not use in the eyes over large areas of the body on individuals who are allergic or sensitive to iodine Ask a doctor before use if you have deep or puncture wounds, animal bites serious burns When using this product do not use longer than one wek unless directed by a doctor Stop use and ask a doctor if conditions persists or gets worse irritation and redness develops

Reported adverse events (FAERS/openFDA)#

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