FDA label 891a69a7-e046-c8c5-e053-2995a90ab49e

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: 891a69a7-e045-c8c5-e053-2995a90ab49e
SPL ID: 891a69a7-e046-c8c5-e053-2995a90ab49e
Version: 1
Effective date: 2019-05-17
Source export date: 2026-10-30
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:46:15

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		891a69a7-e046-c8c5-e053-2995a90ab49e	id
spl set id		891a69a7-e045-c8c5-e053-2995a90ab49e	set_id

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

Sincerus Florida, LLC. Adverse reactions sf

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