FDA label d41a23a8-0dc6-4b55-8e2d-c8096e5e002b

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
cd5c9342-a67e-4893-91ea-401820ba2ba9
SPL ID
d41a23a8-0dc6-4b55-8e2d-c8096e5e002b
Version
4
Effective date
2011-09-22
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 01:42:39

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 TO AVOID CONTAMINATION, DO NOT TOUCH TIP OF CONTAINER TO ANY SURFACE. ONCE OPENED, DISCARD. IF YOU EXPERIENCE EYE PAIN, CHANGES IN VISION, CONTINUED REDNESS OR IRRITATION OF THE EYE, OR IF THE CONDITION WORSENS OR PERSISTS CONSULT A DOCTOR. OBTAIN IMMEDIATE MEDICAL TREATMENT FOR ALL OPEN WOUNDS IN OR NEAR THE EYES. IF SOLUTION CHANGES COLOR OR BECOMES CLOUDY DO NOT USE.

Reported adverse events (FAERS/openFDA)#

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