FDA label db5d0166-9806-3a8a-e053-2995a90adad6

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: 4a0c5bf2-e81d-4ffe-bf63-789cf4864f70
SPL ID: db5d0166-9806-3a8a-e053-2995a90adad6
Version: 3
Effective date: 2022-03-29
Source export date: 2026-10-30
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/2026-10-30/9dea423b9e87a781c152bc6e136923fb91acb0732a7a0ec0d2a51142148f160c/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:40:51

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		db5d0166-9806-3a8a-e053-2995a90adad6	id
spl set id		4a0c5bf2-e81d-4ffe-bf63-789cf4864f70	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

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