FDA label e453932f-7a53-4732-81fd-f053440be1aa

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: 4ee3e461-1855-4f10-878b-ca7a647ccdf1
SPL ID: e453932f-7a53-4732-81fd-f053440be1aa
Version: 1
Effective date: 2013-08-02
Source export date: 2026-10-22
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-22/caf5811f980ee3e51e5ea59ba12f125bb3738ddeec8265aac8812df797bc62f1/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run: 20261023T001338Z
Imported at: 2026-10-23 00:29:19

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		e453932f-7a53-4732-81fd-f053440be1aa	id
spl set id		4ee3e461-1855-4f10-878b-ca7a647ccdf1	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

If no improvement is seen after 7 days or new symptoms develop, discontinue use.

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