FDA label 75aa15b2-8ee6-47a5-98c0-009710ec2145

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: ebb98e76-8ca9-4542-bfa0-0681725517f2
SPL ID: 75aa15b2-8ee6-47a5-98c0-009710ec2145
Version: 2
Effective date: 2026-10-13
Source export date: 2026-10-22
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-22/900f57228a266ed4fd8a11e78d75ce718639346ea99b90befe9f294809712917/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run: 20261023T001338Z
Imported at: 2026-10-23 00:45:26

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		75aa15b2-8ee6-47a5-98c0-009710ec2145	id
spl set id		ebb98e76-8ca9-4542-bfa0-0681725517f2	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

Warning Stop use and ask a 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.