Quality Choice Urinary Pain Relief

Product NDC: 83324-201
Requested package NDC: 83324-201-30
11-digit product format: 833240201
Labeler code: 83324
Product ID: 83324-201_79ec9cb2-5205-4e0a-9a82-35c5cdc77a74
Type: HUMAN OTC DRUG
Nonproprietary name: PHENAZOPYRIDINE HYDROCHLORIDE
Dosage form: TABLET
Route: ORAL
Labeler: Chain Drug Marketing Association
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2025-12-02
Substance: PHENAZOPYRIDINE HYDROCHLORIDE
Active strength: 95 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
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: Quality Choice Urinary Pain Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PHENAZOPYRIDINE HYDROCHLORIDE	95 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
1094126	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
45e0cc2f-4a25-40ef-86ed-d1212815d751	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83324-201-30	Quality Choice Urinary Pain Relief	30 in 1 BLISTER PACK	TABLET	30		1
83324-201-30	Quality Choice Urinary Pain Relief	1 in 1 CARTON	TABLET	1		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
Quality Choice Urinary Pain Relief	PHENAZOPYRIDINE HYDROCHLORIDE	Chain Drug Marketing Association	45e0cc2f-4a25-40ef-86ed-d1212815d751	2025-12-02	Warnings	Exact identifier ndc (package): 83324-201-30 ndc (product): 83324-201 ndc11 (package): 83324020130

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
1094126	phenazopyridine HCl 95 MG Oral Tablet	PSN	45e0cc2f-4a25-40ef-86ed-d1212815d751	1
1094126	phenazopyridine hydrochloride 95 MG Oral Tablet	SCD	45e0cc2f-4a25-40ef-86ed-d1212815d751	1
1094126	phenazopyridine HCl 95 MG Oral Tablet	SY	45e0cc2f-4a25-40ef-86ed-d1212815d751	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83324-201-30	83324020130	1 BLISTER PACK in 1 CARTON (83324-201-30) / 30 TABLET in 1 BLISTER PACK	1 blister pack	2025-12-02	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DRUG FACTS	Chain Drug Marketing Association \| Reese Pharmaceutical Co	2025-12-02	HUMAN OTC DRUG LABEL	1