FDA label 01f574ac-e423-cad4-e063-6394a90ae732

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: 48dac324-db4a-42a7-b251-7c974fd17d5e
SPL ID: 01f574ac-e423-cad4-e063-6394a90ae732
Version: 3
Effective date: 2023-08-02
Source export date: 2026-10-23
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/2026-10-23/fb8b67503658e1e31be677f36f2ff17f62c12f6e6e43cdb60667998d168ff110/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 003b0607e7bf4d3ce17ccc0942e221303b4f62b17a6a00c54547eda454293380
Import run: 20261026T035824Z
Imported at: 2026-10-26 04:34:15

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		01f574ac-e423-cad4-e063-6394a90ae732	id
spl set id		48dac324-db4a-42a7-b251-7c974fd17d5e	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

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