Home NDC 73712-114 Uqora Maximum UTI Pain Relief
Product NDC 73712-114
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 Additional Listing Data#
Finished product Yes
Brand name base Uqora Maximum UTI Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENAZOPYRIDINE HYDROCHLORIDE 99.5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0EWG668W17 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1094147 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73712-114-12 Uqora Maximum UTI Pain Relief 1 in 1 CARTON TABLET 1 1 73712-114-12 Uqora Maximum UTI Pain Relief 12 in 1 BLISTER PACK TABLET 12 1 73712-114-12 Uqora Maximum UTI Pain Relief and Flush Convenience Bundle 12 in 1 BLISTER PACK TABLET 12 99.5 mg 1 73712-114-12 Uqora Maximum UTI Pain Relief and Flush Convenience Bundle 1 in 1 CARTON TABLET 99.5 mg 1 73712-114-12 All-In-One UTI Emergency Kit 12 in 1 BLISTER PACK TABLET 12 99.5 mg 1 73712-114-12 All-In-One UTI Emergency Kit 1 in 1 CARTON TABLET 99.5 mg 1 73712-114-24 Uqora Maximum UTI Pain Relief 1 in 1 CARTON TABLET 1 1 73712-114-24 Uqora Maximum UTI Pain Relief 24 in 1 BLISTER PACK TABLET 24 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 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73712-114-12 73712011412 1 BLISTER PACK in 1 CARTON (73712-114-12) / 12 TABLET in 1 BLISTER PACK 1 blister pack 2025-10-27 No No Current 73712-114-24 73712011424 1 BLISTER PACK in 1 CARTON (73712-114-24) / 24 TABLET in 1 BLISTER PACK 1 blister pack 2025-10-27 No No Current