FDA.reportPublic FDA data

FDA label 9c286f03-fd08-486f-9e2b-96e8208cc927

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
112c7b4e-c8e4-4b86-a006-c48f9ddbadc8
SPL ID
9c286f03-fd08-486f-9e2b-96e8208cc927
Version
4
Effective date
2013-08-20
Source export date
2026-10-12
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/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:22:54

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. Replace cap after using. Discard 30 days after opening. Do not use if liquid changes color or becomes cloudy. Stop use and ask a doctor if you feel eye pain, vision changes, continued redness or irritation of the eye, or if condition worsens or lasts for more than 72 hours. Keep out of children's reach. In case of ingestion, seek professional help directly or contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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