FDA label 4e7965f2-09c2-6f9a-e054-00144ff8d46c

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
e200e1ce-94db-48be-b950-39948689b9a0
SPL ID
4e7965f2-09c2-6f9a-e054-00144ff8d46c
Version
3
Effective date
2017-05-01
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:36

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 Avoid contact with the eyes. If contact occurs, flush eyes with water ​Flammable, keep away from fire or flame. ​Do not use With electrocautery procedures In the eyes ​Stop use and ask a doctor if Irritation and redness develops If condition persists for more than 72 hours, consult a physician ​Discontinue use and consult a healthcare practitioner if Irritation develops ​Keep out of reach of children If swallowed, 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.