FDA label fbbe93f1-0d41-4a4a-9c3b-a88583a53787

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: ac37536d-36dc-4e54-a8fe-2888129f7438
SPL ID: fbbe93f1-0d41-4a4a-9c3b-a88583a53787
Version: 1
Effective date: 2018-06-01
Source export date: 2026-11-06
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:30:08

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		fbbe93f1-0d41-4a4a-9c3b-a88583a53787	id
spl set id		ac37536d-36dc-4e54-a8fe-2888129f7438	set_id

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

Warnings If symptoms persist or worsen, seek advice of a physician. If pregnant or breast-feeding, ask a healthcare professional before use.

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