NDC11 73712011412

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
73712-0114-12	73712-0114
73712-114-12	73712-114

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 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
All-In-One UTI Emergency Kit	METHENAMINE, SODIUM SALICYLATE, AND PHENAZOPYRIDINE HYDROCHLORIDE	Bonafide Health, LLC dba Uqora	434652a1-583e-d6f7-e063-6394a90aab8a	2025-11-10	Warnings	Exact identifier ndc (package): 73712-114-12 ndc11 (package): 73712011412
Uqora Maximum UTI Pain Relief and Flush Convenience Bundle	PHENAZOPYRIDINE HYDROCHLORIDE	Bonafide Health, LLC dba Uqora	4354dcce-6d85-4584-e063-6294a90a5616	2025-11-10	Warnings	Exact identifier ndc (package): 73712-114-12 ndc11 (package): 73712011412
Uqora Maximum UTI Pain Relief	PHENAZOPYRIDINE HYDROCHLORIDE	Bonafide Health, LLC dba Uqora	426317e7-a925-116a-e063-6294a90a52dc	2025-10-27	Warnings	Exact identifier ndc (package): 73712-114-12 ndc (product): 73712-114 ndc11 (package): 73712011412

Reported adverse events (FAERS/openFDA)#

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