FDA label 8738d91c-e670-0a37-e053-2991aa0a663e

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: 8738d91c-e66f-0a37-e053-2991aa0a663e
SPL ID: 8738d91c-e670-0a37-e053-2991aa0a663e
Version: 1
Effective date: 2019-04-23
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:10:44

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		8738d91c-e670-0a37-e053-2991aa0a663e	id
spl set id		8738d91c-e66f-0a37-e053-2991aa0a663e	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. x

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