FDA label ad451d2e-292a-42db-8b48-0a98e11637da

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: a8698abf-78fe-4904-8105-3f46687b4ce3
SPL ID: ad451d2e-292a-42db-8b48-0a98e11637da
Version: 1
Effective date: 2012-05-23
Source export date: 2026-11-06
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:06:31

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		ad451d2e-292a-42db-8b48-0a98e11637da	id
spl set id		a8698abf-78fe-4904-8105-3f46687b4ce3	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

Hypersensivity may result in the area of application, not consume this product, if swallowed consult your doctor.

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