NDC 59368-393 - 24 HOUR ALLERGY

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 59368-393
Package NDCs from labels: 59368-393-01, 59368-393-02
Manufacturer: Praxis, LLC
Effective date: 2023-01-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
24 HOUR ALLERGY - Praxis, LLC	Praxis, LLC	2023-01-01	HUMAN OTC DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 45 of 45 · 882 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cetirizine Hydrochloride	CETIRIZINE HYDROCHLORIDE	Sandoz Inc	760dd0e4-280a-4d95-8938-cecaa7ec75f2	2013-06-03	Warnings	Exact identifier unii: 64O047KTOA
Cetirizine Hydrochloride	CETIRIZINE HYDROCHLORIDE	Dr.Reddy's Laboratories Limited	de152651-bfcd-856a-8329-a2ac93a376bc	2011-09-30	Warnings	Exact identifier unii: 64O047KTOA

Reported adverse events (FAERS/openFDA)#

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