FDA label 5f833faf-65b5-413e-91ff-e24f328adfe4

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: 8af77afe-7359-4992-a7b5-4f9c68630c1a
SPL ID: 5f833faf-65b5-413e-91ff-e24f328adfe4
Version: 2
Effective date: 2011-09-07
Source export date: 2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:21:59

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		5f833faf-65b5-413e-91ff-e24f328adfe4	id
spl set id		8af77afe-7359-4992-a7b5-4f9c68630c1a	set_id

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

Adverse Reactions Nausea, abdominal cramps, and diarrhea have been reported in patients on doses over 3 g daily.

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