FDA label b8bff17c-747c-4819-9d1a-579a1bedbc90

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
5ff6cec8-1659-4d37-a614-70539689a348
SPL ID
b8bff17c-747c-4819-9d1a-579a1bedbc90
Version
3
Effective date
2023-05-15
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:44:27

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 this product if solution changes color or becomes cloudy Stop use and ask a doctor 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 When using this product • to avoid contamination, do not touch tip of container to any surface • replace cap after using. Keep container tightly closed. • remove contact lens before using Keep out of the reach of children. If accidentally 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.