FDA label 7d9025e5-ddd4-5e94-e053-2991aa0a439c

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: 46a655c9-0391-46c8-af77-d0a11bac9557
SPL ID: 7d9025e5-ddd4-5e94-e053-2991aa0a439c
Version: 4
Effective date: 2018-12-21
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:50:53

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		7d9025e5-ddd4-5e94-e053-2991aa0a439c	id
spl set id		46a655c9-0391-46c8-af77-d0a11bac9557	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. When using this product; Do not use in eyes. Discontinue use if irritation and redness develop

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