FDA.reportPublic FDA data

FDA label aa1469b3-6e8a-418f-a110-755a24d8fe9a

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
bfac34cc-05bd-46fb-9fb0-c15bc31c76be
SPL ID
aa1469b3-6e8a-418f-a110-755a24d8fe9a
Version
2
Effective date
2015-11-11
Source export date
2026-11-06
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:57:30

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 When using this product Avoid contact with the eyes Do not use in large quantities particularly over raw surfaces or blistered areas. Do not exceed recommended dosage unless directed by a doctor Stop use and ask a doctor if allergic reaction occurs condition worsens or does not improve within 7 days Symptoms clear up and return within a few days notice any unusual effects such as blurred vision, dizziness or drowsiness, difficulty in breathing, trembling, chest pain or irregular heart beat

Reported adverse events (FAERS/openFDA)#

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