FDA label 4b26437a-7999-4ae7-99a7-5bbbc01e6300

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: 03f6044f-2cd0-47b7-ae5e-5fa287994df3
SPL ID: 4b26437a-7999-4ae7-99a7-5bbbc01e6300
Version: 1
Effective date: 2011-07-27
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:07:32

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		4b26437a-7999-4ae7-99a7-5bbbc01e6300	id
spl set id		03f6044f-2cd0-47b7-ae5e-5fa287994df3	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

Warnings: For external use only. Avoid contact with eyes. Discontinue use if signs of irritation appear.

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