NDC 61715-033-32 - Preferred Plus Urinary Pain Relief

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: 61715-033
Requested NDC: 61715-033-32
Package NDCs from labels: 61715-033-32, 61715-033-01
Manufacturer: Kinray | Reese Pharmaceutical Co
Effective date: 2013-03-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Preferred Plus Urinary Pain Relief - Kinray \| Reese Pharmaceutical Co	Kinray \| Reese Pharmaceutical Co	2013-03-01	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61715-033-01	2020-02-13	C162847	48780-1	9d75b9d1-0b73-f424-e053-dadaa90a57ce	DRUG FACTS
61715-033-01	2020-01-31	C162847	48780-1	9d75b9d1-0b73-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PHENAZOPYRIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	0EWG668W17	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
PHENAZOPYRIDINE	ACTIVE MOIETY	K2J09EMJ52	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
CARNAUBA WAX	INACTIVE INGREDIENT	R12CBM0EIZ	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
MAGNESIUM SILICATE	INACTIVE INGREDIENT	9B9691B2N9	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	PREFERRED PLUS URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KINRAY]	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 8 · 156 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE HYDROCHLORIDE	REMEDYREPACK INC.	49baf6e5-133a-4e1a-9740-506673d27caf	2026-08-21	Warnings, Adverse reactions	Exact identifier unii: 0EWG668W17
Rohto All-In-One	HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE	The Mentholatum Company	43e690e4-b381-46e3-838c-33aef5bdadde	2026-08-20	Warnings	Exact identifier unii: 3NXW29V3WO
Leader Dry Eye Relief Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	CARDINAL HEALTH 110, LLC. DBA LEADER	2ded4bda-b3c3-4521-8701-5c8446fd148b	2026-08-17	Warnings	Exact identifier unii: 3NXW29V3WO
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE	Preferred Pharmaceuticals Inc.	c0e5d32e-075f-4c76-8332-a06560001efe	2026-08-14	Adverse reactions	Exact identifier unii: 0EWG668W17
Dr. Shitong Photon Energy Eye Care Liquid	TETRAHYDROZOLINE HCL 0.05% HYPROMELLOSE 0.3% DR. SHITONG PHOTON ENERGY EYE CARE LIQUID	Wenzhou Yuyuan Pharmaceutical Co., Ltd.	58ace434-55ef-17ef-e063-6294a90aa878	2026-08-10	Warnings	Exact identifier unii: 3NXW29V3WO
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE	REMEDYREPACK INC.	f6829698-b12e-484d-a322-d2f68586e637	2026-08-07	Adverse reactions	Exact identifier unii: 0EWG668W17
Gencare-Urinary Pain Relief Maximum Strength	PHENAZOPYRIDINE HYDROCHLORIDE	Pioneer Life Sciences, LLC	6bbf15b4-2954-40ff-8460-1ef0ed890654	2026-08-03	Warnings	Exact identifier unii: 0EWG668W17
Nuvicare-Urinary Pain Relief Maximum Strength	PHENAZOPYRIDINE HYDROCHLORIDE	NUVICARE LLC	5fe4e4dc-f1c4-4617-b6a6-6ea16a63abfe	2026-08-03	Warnings	Exact identifier unii: 0EWG668W17
Cystex Max Strength UTI Pain Relief	CYSTEX MAX STRENGTH UTI PAIN RELIEF	Clarion Brands LLC	57482f71-80d3-b20d-e063-6394a90a0cf4	2026-07-27	Warnings	Exact identifier unii: 0EWG668W17
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE HYDROCHLORIDE	REMEDYREPACK INC.	6eb59b69-4ad0-47b1-bd3c-1d04d0852ec5	2026-07-27	Warnings, Adverse reactions	Exact identifier unii: 0EWG668W17
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE HYDROCHLORIDE	NuCare Pharmaceuticals, Inc.	56ad921f-0b6e-aa2b-e063-6394a90aec6b	2026-07-15	Warnings, Adverse reactions	Exact identifier unii: 0EWG668W17
PHENAZOPYRIDINE HYDROCHLORIDE	PHENAZOPYRIDINE HYDROCHLORIDE	Genus Lifesciences Inc.	991b3b97-9cea-4c48-90a4-ebff55417d98	2026-07-14	Adverse reactions	Exact identifier unii: 0EWG668W17
Artificial Tears	ARTIFICIAL TEARS	AvPAK	f18bebf2-1936-658f-e053-2a95a90a5012	2026-07-07	Warnings	Exact identifier unii: 3NXW29V3WO
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE HYDROCHLORIDE	REMEDYREPACK INC.	7e131f69-d259-404d-a859-0497f5cbe856	2026-06-24	Adverse reactions	Exact identifier unii: 0EWG668W17
Rohto Sun and Sport	HYPROMELLOSE, POVIDONE	The Mentholatum Company	8bcc8882-b886-4b55-9bc4-d4b92a41358f	2026-06-19	Warnings	Exact identifier unii: 3NXW29V3WO
Rohto Dual Light Relief	HYPROMELLOSE, POVIDONE	The Mentholatum Company	1b597f83-d7f1-cf93-e063-6394a90a99f7	2026-06-19	Warnings	Exact identifier unii: 3NXW29V3WO
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE HYDROCHLORIDE	NuCare Pharmaceuticals, Inc.	548edf26-c81e-f982-e063-6394a90af9da	2026-06-18	Warnings, Adverse reactions	Exact identifier unii: 0EWG668W17
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE	REMEDYREPACK INC.	82dc87bb-ba27-4b86-9bc9-18492975ac9f	2026-06-10	Adverse reactions	Exact identifier unii: 0EWG668W17
Preferred Maximum Strength Urinary Pain Relief	PHENAZOPYRIDINE HYDROCHLORIDE	Preferred Pharmaceuticals Inc.	0fa8638c-e3e0-4bbf-9101-842e5d8736d6	2026-06-04	Warnings	Exact identifier unii: 0EWG668W17
Rohto Digi-Eye	HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE	The Mentholatum Company	5d6f37b9-b568-4cb6-92de-eb40779f3f8c	2026-06-03	Warnings	Exact identifier unii: 3NXW29V3WO

Reported adverse events (FAERS/openFDA)#

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