Home NDC 41250-557 Meijer Antibacterial Plus Urinary Pain Relief
Product NDC 41250-557
11-digit product format 412500557
Labeler code 41250
Product ID 41250-557_06ba68f7-27f0-4e27-9216-2b1e620febea
Type HUMAN OTC DRUG
Nonproprietary name METHENAMINE, SODIUM SALICYLATE
Dosage form TABLET
Route ORAL
Labeler Meijer Distribution Inc.
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 Meijer 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 41250-557-24 Meijer Antibacterial Plus Urinary Pain Relief 1 in 1 CARTON TABLET 1 6 41250-557-24 Meijer Antibacterial Plus Urinary Pain Relief 24 in 1 BLISTER PACK TABLET 24 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-557 MEIJER ANTIBACTERIAL PLUS URINARY PAIN RELIEF (METHENAMINE, SODIUM SALICYLATE) TABLET [MEIJER DISTRIBUTION INC.] 6 Current NDC, Legacy NDC, 2 package rows 20241220_9eaaf197-9e96-4220-b49d-2f743b443623.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 41250-557-24 41250055724 1 BLISTER PACK in 1 CARTON (41250-557-24) / 24 TABLET in 1 BLISTER PACK 1 blister pack 2017-02-22 0000-00-00 No No Current