FDA label 28abfd0f-c73f-4b4d-843f-b0dec6534769

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
634dc331-5532-4303-a725-1f786101e555
SPL ID
28abfd0f-c73f-4b4d-843f-b0dec6534769
Version
5
Effective date
2024-05-21
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:14:31

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 (in the eye) Wait at least 15 minutes between using two different eye products. Use this gel last. Do not use if you are allergic to any of the ingredients. If solution changes color or becomes cloudy, do not use. Do not use if the pouch or vial is damaged. To avoid contamination, do not touch the tip of container to any surface. Do not reuse. Once opened, discard. Store below 77°F. Expiration date refers to the product in intact packaging, stored correctly. If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor. If pregnant , trying to get pregnant or breast feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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