FDA label b8e83fe2-9685-4941-8956-90f5a196830a

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: 8080a78d-30fe-4155-817f-354131aa652b
SPL ID: b8e83fe2-9685-4941-8956-90f5a196830a
Version: 3
Effective date: 2026-10-12
Source export date: 2026-10-23
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/2026-10-23/d2cd0a09965f36e77971cde2bab1b507527edc75cafd1ad7d62ff9dc1c8d1c84/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 003b0607e7bf4d3ce17ccc0942e221303b4f62b17a6a00c54547eda454293380
Import run: 20261026T035824Z
Imported at: 2026-10-26 04:45:41

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		b8e83fe2-9685-4941-8956-90f5a196830a	id
spl set id		8080a78d-30fe-4155-817f-354131aa652b	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 Stop use and ask your doctor if symptoms persist or worsen. If pregnant or breast-feeding, take only on advice of a healthcare professional.

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