FDA label c40af21f-8949-49ac-a5c9-28e4edd6288d

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: 0d643110-3a27-4297-bab9-bb621f0bcf27
SPL ID: c40af21f-8949-49ac-a5c9-28e4edd6288d
Version: 2
Effective date: 2017-03-08
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:49:48

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		c40af21f-8949-49ac-a5c9-28e4edd6288d	id
spl set id		0d643110-3a27-4297-bab9-bb621f0bcf27	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 breastfeeding, take only on advice of a healthcare professional.

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