FDA.reportPublic FDA data

Uqora Maximum UTI Pain Relief

Product NDC
73712-114
Requested package NDC
73712-114-12
11-digit product format
737120114
Labeler code
73712
Product ID
73712-114_426317e7-a926-116a-e063-6294a90a52dc
Type
HUMAN OTC DRUG
Nonproprietary name
PHENAZOPYRIDINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bonafide Health, LLC dba Uqora
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-10-27
Substance
PHENAZOPYRIDINE HYDROCHLORIDE
Active strength
99.5 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
Uqora Maximum UTI Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHENAZOPYRIDINE HYDROCHLORIDE99.5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0EWG668W17Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

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

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
426317e7-a925-116a-e063-6294a90a52dcAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
260b0da6-d3d7-262f-a60f-d4b36d5f1b4dProduct name620251210
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73712-114-12Uqora Maximum UTI Pain Relief1 in 1 CARTONTABLET11
73712-114-12Uqora Maximum UTI Pain Relief12 in 1 BLISTER PACKTABLET121
73712-114-12Uqora Maximum UTI Pain Relief and Flush Convenience Bundle12 in 1 BLISTER PACKTABLET1299.5 mg1
73712-114-12Uqora Maximum UTI Pain Relief and Flush Convenience Bundle1 in 1 CARTONTABLET99.5 mg1
73712-114-12All-In-One UTI Emergency Kit12 in 1 BLISTER PACKTABLET1299.5 mg1
73712-114-12All-In-One UTI Emergency Kit1 in 1 CARTONTABLET99.5 mg1
73712-114-24Uqora Maximum UTI Pain Relief1 in 1 CARTONTABLET11
73712-114-24Uqora Maximum UTI Pain Relief24 in 1 BLISTER PACKTABLET241

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
All-In-One UTI Emergency KitMETHENAMINE, SODIUM SALICYLATE, AND PHENAZOPYRIDINE HYDROCHLORIDEBonafide Health, LLC dba Uqora434652a1-583e-d6f7-e063-6394a90aab8a2025-11-10WarningsExact identifier
ndc (package): 73712-114-12
ndc11 (package): 73712011412
Uqora Maximum UTI Pain Relief and Flush Convenience BundlePHENAZOPYRIDINE HYDROCHLORIDEBonafide Health, LLC dba Uqora4354dcce-6d85-4584-e063-6294a90a56162025-11-10WarningsExact identifier
ndc (package): 73712-114-12
ndc11 (package): 73712011412
Uqora Maximum UTI Pain ReliefPHENAZOPYRIDINE HYDROCHLORIDEBonafide Health, LLC dba Uqora426317e7-a925-116a-e063-6294a90a52dc2025-10-27WarningsExact identifier
ndc (package): 73712-114-12
ndc (product): 73712-114
ndc11 (package): 73712011412

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1489932methenamine 162 MG / sodium salicylate 162.5 MG Oral TabletPSN434652a1-583e-d6f7-e063-6394a90aab8a1
1094147phenazopyridine HCl 99.5 MG Oral TabletPSN426317e7-a925-116a-e063-6294a90a52dc1
1094147phenazopyridine HCl 99.5 MG Oral TabletPSN434652a1-583e-d6f7-e063-6394a90aab8a1
1094147phenazopyridine HCl 99.5 MG Oral TabletPSN4354dcce-6d85-4584-e063-6294a90a56161
1489932methenamine 162 MG / sodium salicylate 162.5 MG Oral TabletSCD434652a1-583e-d6f7-e063-6394a90aab8a1
1094147phenazopyridine hydrochloride 99.5 MG Oral TabletSCD426317e7-a925-116a-e063-6294a90a52dc1
1094147phenazopyridine hydrochloride 99.5 MG Oral TabletSCD434652a1-583e-d6f7-e063-6394a90aab8a1
1094147phenazopyridine hydrochloride 99.5 MG Oral TabletSCD4354dcce-6d85-4584-e063-6294a90a56161
1094147phenazopyridine HCl 99.5 MG Oral TabletSY426317e7-a925-116a-e063-6294a90a52dc1
1094147phenazopyridine HCl 99.5 MG Oral TabletSY434652a1-583e-d6f7-e063-6394a90aab8a1
1094147phenazopyridine HCl 99.5 MG Oral TabletSY4354dcce-6d85-4584-e063-6294a90a56161

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73712-114-12737120114121 BLISTER PACK in 1 CARTON (73712-114-12) / 12 TABLET in 1 BLISTER PACK1 blister pack2025-10-27NoNoCurrent