Urinary Pain Relief

Product NDC: 73581-919
Requested package NDC: 73581-919-72
11-digit product format: 735810919
Labeler code: 73581
Product ID: 73581-919_5137d15a-1390-d5f1-e063-6394a90aabfd
Type: HUMAN OTC DRUG
Nonproprietary name: Phenazopyridine Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: YYBA CORP
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2026-04-01
Substance: PHENAZOPYRIDINE HYDROCHLORIDE
Active strength: 99.5 mg/1
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Urinary Pain Relief
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PHENAZOPYRIDINE HYDROCHLORIDE	99.5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
0EWG668W17	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1094147	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
f2d9f6aa-081e-4723-9417-5191b31d2952	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73581-919-12	Urinary Pain Relief	120 in 1 BOTTLE	TABLET	120	1
73581-919-36	Urinary Pain Relief	36 in 1 BOTTLE	TABLET	36	1
73581-919-72	Urinary Pain Relief	72 in 1 BOTTLE	TABLET	72	1

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Urinary Pain Relief	PHENAZOPYRIDINE HYDROCHLORIDE	YYBA CORP	f2d9f6aa-081e-4723-9417-5191b31d2952	2026-04-01	Warnings	Exact identifier ndc (package): 73581-919-72 ndc (product): 73581-919 ndc11 (package): 73581091972

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
0EWG668W17	PHENAZOPYRIDINE HYDROCHLORIDE	136-40-3	PHENAZOPYRIDINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1094147	phenazopyridine HCl 99.5 MG Oral Tablet	PSN	f2d9f6aa-081e-4723-9417-5191b31d2952	1
1094147	phenazopyridine hydrochloride 99.5 MG Oral Tablet	SCD	f2d9f6aa-081e-4723-9417-5191b31d2952	1
1094147	phenazopyridine HCl 99.5 MG Oral Tablet	SY	f2d9f6aa-081e-4723-9417-5191b31d2952	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
73581-919-72	73581091972	72 TABLET in 1 BOTTLE (73581-919-72)	72 tablet	2026-04-01	No	No	Current