FDA label c80f9eee-4083-4aef-8553-5e25848ec7ce

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: 539efeee-7822-43ad-b85c-ae63a5a8b3a5
SPL ID: c80f9eee-4083-4aef-8553-5e25848ec7ce
Version: 3
Effective date: 2010-10-20
Source export date: 2026-11-06
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:53:14

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		c80f9eee-4083-4aef-8553-5e25848ec7ce	id
spl set id		539efeee-7822-43ad-b85c-ae63a5a8b3a5	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

WARNING: Stop use if skin rash occurs.

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