Home NDC 11822-4892 Rite Aid Antibacterial Plus Urinary Pain Relief
Product NDC 11822-4892
11-digit product format 118224892
Labeler code 11822
Product ID 11822-4892_16b04fae-6704-40f9-b58d-8caa148df96c
Type HUMAN OTC DRUG
Nonproprietary name METHENAMINE, SODIUM SALICYLATE
Dosage form TABLET
Route ORAL
Labeler Rite Aid
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2017-02-22
Substance METHENAMINE; SODIUM SALICYLATE
Active strength 162; 162.5 mg/1; 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 Rite Aid Antibacterial Plus Urinary Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHENAMINE 162 mg/1 SODIUM SALICYLATE 162.5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination J50OIX95QV Internal UNII lookup WIQ1H85SYP Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1489932 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 11822-4892-4 Rite Aid Antibacterial Plus Urinary Pain Relief 24 in 1 BLISTER PACK TABLET 24 3 11822-4892-4 Rite Aid Antibacterial Plus Urinary Pain Relief 1 in 1 CARTON TABLET 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-4892 RITE AID ANTIBACTERIAL PLUS URINARY PAIN RELIEF (METHENAMINE, SODIUM SALICYLATE) TABLET [RITE AID] 3 Current NDC, Legacy NDC, 2 package rows 20241220_b683cfe1-43e0-4111-bd4c-ebb15fef829b.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 Marketing end Sample Exclude flag Status 11822-4892-4 11822489204 1 BLISTER PACK in 1 CARTON (11822-4892-4) / 24 TABLET in 1 BLISTER PACK 1 blister pack 2017-02-22 0000-00-00 No No Current