FDA label 167fb8c2-547b-4c4d-88ed-9b5ac95128e5

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
3b3c3bf3-0be8-4810-9ef2-3c8866e45578
SPL ID
167fb8c2-547b-4c4d-88ed-9b5ac95128e5
Version
5
Effective date
2020-10-21
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:09

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 Do not use this product except under the advice and supervision of a doctor if imprinted seal on bottle is missing or broken if solution changes color or becomes cloudy When using this product temporary burning and irritation upon being instilled into eye may occur to avoid contamination, do not touch tip of container to any surface replace cap after each use Stop use and ask a doctor if you experience eye pain you experience changes in vision redness or irritation of the eye continues condition worsens or persists Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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