FDA label a238b922-010a-40fb-8ee8-da3a82c376c4

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
dbb0d312-c79a-4c89-acb1-b895b52c05d5
SPL ID
a238b922-010a-40fb-8ee8-da3a82c376c4
Version
1
Effective date
2009-08-31
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:49

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 To avoid contamination replace cap after use Do not touch the tip of the container to any surface to avoid contamination Do not use 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, or if condition persists for more than 72 hours or worsens Keep this and all other drugs out of the reach of children

Reported adverse events (FAERS/openFDA)#

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