FDA label 7256a740-d931-11de-ae13-0002a5d5c51b

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
6d4ecfc0-d931-11de-beed-0002a5d5c51b
SPL ID
7256a740-d931-11de-ae13-0002a5d5c51b
Version
1
Effective date
2009-11-30
Source export date
2026-11-06
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:06:25

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: - Side effects may include headahce, nausea, sore throat, allergic rhinitis and gastointestinal upset. - If symptoms persist or worsen, stop using this product and consult a physician. - When Using This Product: avoid contact with the eyes. If product gets into eyes, flush with water. Seek medical attention.

Reported adverse events (FAERS/openFDA)#

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