FDA label cb3c7fda-f6e6-4520-9a01-017a9368f99f

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: 0b217365-aa8e-4fa9-9446-36e1cd265639
SPL ID: cb3c7fda-f6e6-4520-9a01-017a9368f99f
Version: 4
Effective date: 2013-01-30
Source export date: 2026-11-06
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:48:15

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		cb3c7fda-f6e6-4520-9a01-017a9368f99f	id
spl set id		0b217365-aa8e-4fa9-9446-36e1cd265639	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, consult a healthcare professional

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