FDA label 915ca54e-71c0-48a9-a6a6-43b9efc25ec1

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: a0387018-5570-4452-957d-7569eea7eaa1
SPL ID: 915ca54e-71c0-48a9-a6a6-43b9efc25ec1
Version: 3
Effective date: 2011-11-15
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 02:49:30

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		915ca54e-71c0-48a9-a6a6-43b9efc25ec1	id
spl set id		a0387018-5570-4452-957d-7569eea7eaa1	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.