Maximum Strength Urinary Pain Relief

Product NDC
30142-756
11-digit product format
301420756
Labeler code
30142
Product ID
30142-756_a4a5f566-eb9e-46d1-b93e-f00d32b796ba
Type
HUMAN OTC DRUG
Nonproprietary name
Phenazopyridine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
KROGER COMPANY
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-05-01
Substance
PHENAZOPYRIDINE HYDROCHLORIDE
Active strength
99.5 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Maximum Strength Urinary 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
3334e3f6-f57c-45f9-9fa5-5ea3f93d335aAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-756-24Maximum Strength Urinary Pain Relief1 in 1 CARTONTABLET13
30142-756-24Maximum Strength Urinary Pain Relief24 in 1 BLISTER PACKTABLET243

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-756MAXIMUM STRENGTH URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [KROGER COMPANY]3Current NDC, Legacy NDC, 2 package rows20240113_3334e3f6-f57c-45f9-9fa5-5ea3f93d335a.zip

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
Maximum Strength Urinary Pain ReliefPHENAZOPYRIDINE HYDROCHLORIDEKROGER COMPANY3334e3f6-f57c-45f9-9fa5-5ea3f93d335a2023-12-30WarningsExact identifier
ndc (product): 30142-756

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094147phenazopyridine HCl 99.5 MG Oral TabletPSN3334e3f6-f57c-45f9-9fa5-5ea3f93d335a3
1094147phenazopyridine hydrochloride 99.5 MG Oral TabletSCD3334e3f6-f57c-45f9-9fa5-5ea3f93d335a3
1094147phenazopyridine HCl 99.5 MG Oral TabletSY3334e3f6-f57c-45f9-9fa5-5ea3f93d335a3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-756-24301420756241 BLISTER PACK in 1 CARTON (30142-756-24) / 24 TABLET in 1 BLISTER PACK1 blister pack2021-05-010000-00-00NoNoCurrent