FDA label 45749435-d1b0-e995-e063-6394a90afc2f

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: 5ff48611-c47f-446d-e053-2991aa0ab4de
SPL ID: 45749435-d1b0-e995-e063-6394a90afc2f
Version: 6
Effective date: 2025-12-08
Source export date: 2026-11-06
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/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:15:48

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		45749435-d1b0-e995-e063-6394a90afc2f	id
spl set id		5ff48611-c47f-446d-e053-2991aa0ab4de	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: Consult your health care provider if symptoms persist more than 5 days or worsen.

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