FDA label 4817aae0-ddc5-11de-a5b9-0002a5d5c51b

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: 9ad47340-ddbf-11de-a1c2-0002a5d5c51b
SPL ID: 4817aae0-ddc5-11de-a5b9-0002a5d5c51b
Version: 1
Effective date: 2009-11-30
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:33:42

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		4817aae0-ddc5-11de-a5b9-0002a5d5c51b	id
spl set id		9ad47340-ddbf-11de-a1c2-0002a5d5c51b	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 oral use only. Over use may induce headaches. Not for use by pregnant women. If symptoms persist, consult a physician.

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