FDA.reportPublic FDA data

FDA label 797a200b-7a78-7ab8-e053-2a91aa0abc6f

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
39dbc355-c6f8-3a38-e054-00144ff8d46c
SPL ID
797a200b-7a78-7ab8-e053-2a91aa0abc6f
Version
2
Effective date
2018-10-30
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:50:21

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 - Do not use this product if you have heart disease, high blood pressure, thyroid disease, diabetes, or problems with urination unless directed by a doctor. - Do not use this product if you are presently taking a prescription drug for high blood pressure or depression. - Discontinue use if redness, irritation, swelling, pain, or other symptoms of allergy develop. - Discontinue use if condition worsens and consult a doctor. - Keep out of reach of children - Avoid getting into eyes.

Reported adverse events (FAERS/openFDA)#

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