Home NDC 69693-519-24 Cystex Max Strength UTI Pain Relief
Product NDC 69693-519
Requested package NDC 69693-519-24
11-digit product format 696930519
Labeler code 69693
Product ID 69693-519_57482f71-80d4-b20d-e063-6394a90a0cf4
Type HUMAN OTC DRUG
Nonproprietary name Cystex Max Strength UTI Pain Relief
Dosage form TABLET
Route ORAL
Labeler Clarion Brands LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-27
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 99.5 mg/99.5mg
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Cystex Max Strength UTI Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENAZOPYRIDINE HYDROCHLORIDE 99.5 mg/99.5mg
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.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Status 69693-519-24 69693051924 2 BLISTER PACK in 1 CARTON (69693-519-24) / 99.5 mg in 1 BLISTER PACK 2 blister pack 2026-07-27 0 Current