FDA label f1ed2a28-1ebe-bbb3-e053-2a95a90ae6c5

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
a0fc8525-527a-cedd-e053-2a95a90a8512
SPL ID
f1ed2a28-1ebe-bbb3-e053-2a95a90ae6c5
Version
5
Effective date
2023-01-10
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:46

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 When using this product avoid contamination, do not touch tip of container to any surface replace cap after use. Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye. the condition worsens or persists for more than 72 hours. Keep this and all drugs out of the 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.