Home NDC 70692-178 GOOD REMEDIES Maximum Strength Urinary Pain Relief Caplet
Product NDC 70692-178
11-digit product format 706920178
Labeler code 70692
Product ID 70692-178_3b8052c0-6936-4d15-82f6-885f083694a4
Type HUMAN OTC DRUG
Nonproprietary name Phenazopyridine hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Strive Pharmaceuticals Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-01-06
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 99.5 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base GOOD REMEDIES Maximum Strength Urinary Pain Relief Caplet
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70692-178-08 GOOD REMEDIES Maximum Strength Urinary Pain Relief Caplet 1 in 1 CARTON TABLET, FILM COATED 1 2 70692-178-08 GOOD REMEDIES Maximum Strength Urinary Pain Relief Caplet 8 in 1 BLISTER PACK TABLET, FILM COATED 8 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70692-178 GOOD REMEDIES MAXIMUM STRENGTH URINARY PAIN RELIEF CAPLET (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET, FILM COATED [STRIVE PHARMACEUTICALS INC.] 2 Current NDC, 2 package rows 20250112_269fa921-f4c4-16e7-e063-6394a90a0cbb.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70692-178-08 70692017808 1 BLISTER PACK in 1 CARTON (70692-178-08) / 8 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 2025-01-06 No No Current