FDA label 27eb6e41-bcf1-27f3-e063-6394a90a5ef4

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
d29dc2ae-bfae-4bd0-9863-ae463867e1d9
SPL ID
27eb6e41-bcf1-27f3-e063-6394a90a5ef4
Version
2
Effective date
2024-11-27
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:18:04

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

Warnings For external use only Do not use if this product changes color or becomes cloudy if you are sensitive to any ingredient in this product When using this product to avoid contamination do no touch tip of container to any surface replace cap after each use remove contact lenses before use Stop use and ask a doctor if you experience any of the following: eye pain change in vision continued redness or irritation of the eye condition worsens or persisters for more than 72 hours Keep out of reach of children . If swallowed, get medica-l help or contact a Poison Control Center right (1-800-222-1222) away.

Reported adverse events (FAERS/openFDA)#

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