FDA.reportPublic FDA data

FDA label 49a2fdf9-1bd1-56de-e063-6294a90afdda

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
10c3e31d-779d-8ff6-e063-6294a90acd39
SPL ID
49a2fdf9-1bd1-56de-e063-6294a90afdda
Version
4
Effective date
2026-01-30
Source export date
2026-11-06
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/2026-11-06/d46c999c1947092f6e18e5233482e6d1c02312c89d32ce906e3b19672a696546/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:04:44

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

Warning • For external use only. • To avoid contamination, do not touch tip of container to any surface. • If solution changes color or becomes cloudy, do not use. • Do not use a damaged or punctured single-dose container. • Wait at least 15 minutes between possible applications of other ophthalmic medication. • Use immediately once opened. • Do not reuse. Discard any remaining solution after use. • Do not use if you are sensitive to any of the ingredients. • Do not use after the expiry date shown on the pack.

Reported adverse events (FAERS/openFDA)#

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