FDA.reportPublic FDA data

CVS Maximum Strength Urinary Pain Relief

Product NDC
69842-713
Requested package NDC
69842-713-24
11-digit product format
698420713
Labeler code
69842
Product ID
69842-713_00cc9726-e2b5-4d8a-832e-7ff7698ac871
Type
HUMAN OTC DRUG
Nonproprietary name
PHENAZOPYRIDINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
CVS PHARMACY INC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-09-18
Substance
PHENAZOPYRIDINE HYDROCHLORIDE
Active strength
99.5 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Maximum Strength Urinary Pain ReliefPHENAZOPYRIDINE HYDROCHLORIDECVS PHARMACY INCbddc4208-0559-4f41-a99e-68cfccfade3c2024-12-18WarningsExact identifier
ndc (package): 69842-713-24
ndc (product): 69842-713
ndc11 (package): 69842071324

Additional Listing Data#

Finished product
Yes
Brand name base
CVS 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
bddc4208-0559-4f41-a99e-68cfccfade3cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-713-12CVS Maximum Strength Urinary Pain Relief1 in 1 CARTONTABLET18
69842-713-12CVS Maximum Strength Urinary Pain Relief12 in 1 BLISTER PACKTABLET128
69842-713-24CVS Maximum Strength Urinary Pain Relief1 in 1 CARTONTABLET18
69842-713-24CVS Maximum Strength Urinary Pain Relief24 in 1 BLISTER PACKTABLET248

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-713CVS MAXIMUM STRENGTH URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [CVS PHARMACY INC]8Current NDC, Legacy NDC, 4 package rows20241220_bddc4208-0559-4f41-a99e-68cfccfade3c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094147phenazopyridine HCl 99.5 MG Oral TabletPSNbddc4208-0559-4f41-a99e-68cfccfade3c8
1094147phenazopyridine hydrochloride 99.5 MG Oral TabletSCDbddc4208-0559-4f41-a99e-68cfccfade3c8
1094147phenazopyridine HCl 99.5 MG Oral TabletSYbddc4208-0559-4f41-a99e-68cfccfade3c8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-713-24698420713241 BLISTER PACK in 1 CARTON (69842-713-24) / 24 TABLET in 1 BLISTER PACK1 blister pack2019-09-180000-00-00NoNoCurrent