FDA label 1a0284e5-6109-ba12-e063-6294a90ab265

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
850ae6eb-6f96-3743-e053-2991aa0a513c
SPL ID
1a0284e5-6109-ba12-e063-6294a90ab265
Version
8
Effective date
2024-06-03
Source export date
2026-10-12
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/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:06:42

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only Do not use if you have asthma or emphysema Stop use and ask a doctor if condition persists

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 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.