FDA label 43d81bd9-1bd4-cbb1-e063-6394a90a33c8

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
a3966e61-4668-600e-e053-2995a90a8f3f
SPL ID
43d81bd9-1bd4-cbb1-e063-6394a90a33c8
Version
3
Effective date
2025-11-17
Source export date
2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:27:25

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 • For use in the eye s only. • Retain outer carton for full product drug facts. 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. • condition worsens or persists for more than 72 hours. If pregnant or breast feeding, ask a health professional before use. Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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