FDA label ba379850-6509-433e-b0c3-caf55478e186

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: 781d1ef8-fb71-47ed-92d2-346284c4ac1d
SPL ID: ba379850-6509-433e-b0c3-caf55478e186
Version: 3
Effective date: 2011-11-15
Source export date: 2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:51:41

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		ba379850-6509-433e-b0c3-caf55478e186	id
spl set id		781d1ef8-fb71-47ed-92d2-346284c4ac1d	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

Caution: If symptoms persist or worsen, a health care professional should be consulted.

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