FDA label 87391cb8-def8-a107-e053-2991aa0a561b

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: 87391cb8-def7-a107-e053-2991aa0a561b
SPL ID: 87391cb8-def8-a107-e053-2991aa0a561b
Version: 1
Effective date: 2019-04-23
Source export date: 2026-11-06
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/2026-11-06/8ec9b1418c25a8bb472a36e6bc0b2cbabb210d48d5dd734197e022d21529ed58/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 09:12:42

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		87391cb8-def8-a107-e053-2991aa0a561b	id
spl set id		87391cb8-def7-a107-e053-2991aa0a561b	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. c

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