FDA label 57993cf5-aa8b-4774-e063-6294a90a4d70

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
446ea824-eb9f-53ba-e063-6394a90aeb29
SPL ID
57993cf5-aa8b-4774-e063-6294a90a4d70
Version
2
Effective date
2026-07-27
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:25

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 Warnings For external use only. To avoid contamination, do not touch tip of container to anysurface. Replace cap after using. If solution changes color or becomes cloudy, do not use. Stop use and ask a doctor Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or ff the condition worsens or persists for more than 72 hours. Keep out of reach of children Keep out of reach of children. H swailowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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