FDA label 39f28d7d-7b23-16b5-e063-6394a90abc16

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: 39f28d7d-7b22-16b5-e063-6394a90abc16
SPL ID: 39f28d7d-7b23-16b5-e063-6394a90abc16
Version: 1
Effective date: 2025-07-15
Source export date: 2026-11-06
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/2026-11-06/968b7138703f8100b14008bced2b2a4531f4fab250b207279e9c05eb19608f40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:15:00

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		39f28d7d-7b23-16b5-e063-6394a90abc16	id
spl set id		39f28d7d-7b22-16b5-e063-6394a90abc16	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 For external use only. Avoid direct contact with eyes. Discontinue use if irritation occurs. warning

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