FDA.reportPublic FDA data

UTI EMERGENCY RELIEF

Product NDC
73436-4882
11-digit product format
734364882
Labeler code
73436
Product ID
73436-4882_4ece6e64-c81e-0fa8-e063-6294a90ac6d1
Type
HUMAN OTC DRUG
Nonproprietary name
methenamine, sodium salicylate, and phenazopyridine hydrochloride kit
Dosage form
KIT
Labeler
CADENCE HEALTH, INC.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2026-04-06
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
UTI EMERGENCY RELIEF
Listing expiration
2027-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1094147Internal RxNorm lookup
1489932Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
3a923df5-15ed-404d-8741-33a9793cb7f5Available 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
73436-1221-2UTI EMERGENCY RELIEF12 in 1 BLISTER PACKTABLET12162.5 mg2
73436-1221-2UTI EMERGENCY RELIEF1 in 1 CARTONTABLET162.5 mg2
73436-2441-2UTI EMERGENCY RELIEF1 in 1 CARTONTABLET99.5 mg2
73436-2441-2UTI EMERGENCY RELIEF12 in 1 BLISTER PACKTABLET1299.5 mg2
73436-4882-4UTI EMERGENCY RELIEF1 in 1 CARTONKIT12

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
UTI EMERGENCY RELIEFMETHENAMINE, SODIUM SALICYLATE, AND PHENAZOPYRIDINE HYDROCHLORIDE KITCADENCE HEALTH, INC.3a923df5-15ed-404d-8741-33a9793cb7f52026-04-06WarningsExact identifier
ndc (product): 73436-4882

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1489932methenamine 162 MG / sodium salicylate 162.5 MG Oral TabletPSN3a923df5-15ed-404d-8741-33a9793cb7f52
1094147phenazopyridine HCl 99.5 MG Oral TabletPSN3a923df5-15ed-404d-8741-33a9793cb7f52
1489932methenamine 162 MG / sodium salicylate 162.5 MG Oral TabletSCD3a923df5-15ed-404d-8741-33a9793cb7f52
1094147phenazopyridine hydrochloride 99.5 MG Oral TabletSCD3a923df5-15ed-404d-8741-33a9793cb7f52
1094147phenazopyridine HCl 99.5 MG Oral TabletSY3a923df5-15ed-404d-8741-33a9793cb7f52

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73436-1221-27343612210212 in 1 BLISTER PACKHistorical
73436-2441-2734362441021 in 1 CARTONHistorical
73436-4882-4734364882041 KIT in 1 CARTON (73436-4882-4) * 1 BLISTER PACK in 1 CARTON (73436-1221-2) / 12 TABLET in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (73436-2441-2) / 12 TABLET in 1 BLISTER PACK1 kit2026-04-15NoNoCurrent