FDA label 7e91f7fb-2a2f-4682-e053-2991aa0a1c5c

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: f96495b5-1ffe-432c-adcf-b2db9cfd1405
SPL ID: 7e91f7fb-2a2f-4682-e053-2991aa0a1c5c
Version: 2
Effective date: 2018-12-21
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:22:25

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		7e91f7fb-2a2f-4682-e053-2991aa0a1c5c	id
spl set id		f96495b5-1ffe-432c-adcf-b2db9cfd1405	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 doctor if symptoms worsen or persist more than 3 days

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