FDA label 05414779-f61f-8fa7-e063-6394a90aa034

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: e11f1216-95fc-454e-e053-2995a90a7cf5
SPL ID: 05414779-f61f-8fa7-e063-6394a90aa034
Version: 3
Effective date: 2023-09-13
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:23:04

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		05414779-f61f-8fa7-e063-6394a90aa034	id
spl set id		e11f1216-95fc-454e-e053-2995a90a7cf5	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 a physician if symptoms persist for more than 3 days or worsen.

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