FDA label 6bf86334-3018-707b-e053-2a91aa0aa567

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
b18c4318-4bfe-4fd4-8d31-a43b9711e237
SPL ID
6bf86334-3018-707b-e053-2a91aa0aa567
Version
3
Effective date
2018-05-11
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:21:04

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

there may occurs the case of irritability when applying eye drop or nasal drop do not worry about it because it is caused by the reaction of Iodine But is it possibly think of the susceptibility to Iodine, which seldom occurs. in case of irritability or rash, stop the use immediately and discuss with doctors keep out of the direct sunlight

Reported adverse events (FAERS/openFDA)#

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