Home NDC 50201-4212 Top Value Effervescent Pain Relief
Product NDC 50201-4212
11-digit product format 502014212
Labeler code 50201
Product ID 50201-4212_26d137e5-b5fe-097e-e063-6394a90a91f3
Type HUMAN OTC DRUG
Nonproprietary name Apirin, Citric Acid, Sodium Bicarbonate
Dosage form TABLET, EFFERVESCENT
Route ORAL
Labeler Tower Laboratories Ltd
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2006-12-01
Substance ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE
Active strength 1000; 325; 1916 mg/1; mg/1; mg/1
Pharmacologic classes Acidifying Activity [MoA], Alkalinizing Activity [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cyclooxygenase Inhibitors [MoA], Decreased Coagulation Factor Activity [PE], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 50201-4212 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 50201-4212 50201-4212-0 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base Top Value Effervescent Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 325 mg/1 ANHYDROUS CITRIC ACID 1000 mg/1 SODIUM BICARBONATE 1916 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R16CO5Y76E Internal UNII lookup XF417D3PSL Internal UNII lookup 8MDF5V39QO Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1536675 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 50201-4212-0 Top Value Effervescent Pain Relief 10 in 1 CARTON TABLET, EFFERVESCENT 10 5 50201-4212-0 Top Value Effervescent Pain Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50201-4212 TOP VALUE EFFERVESCENT PAIN RELIEF (APIRIN, CITRIC ACID, SODIUM BICARBONATE) TABLET, EFFERVESCENT [TOWER LABORATORIES LTD] 5 Current NDC, Legacy NDC, 2 package rows 20241212_43c7f435-735c-3fab-e054-00144ff88e88.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 85 · 1,681 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 50201-4212-0 50201421200 10 POUCH in 1 CARTON (50201-4212-0) / 2 TABLET, EFFERVESCENT in 1 POUCH 10 pouch 2014-08-19 0000-00-00 No No Current