Home NDC 85237-1829 Alka-Seltzer Original
Product NDC 85237-1829
11-digit product format 852371829
Labeler code 85237
Product ID 85237-1829_3ca80d7c-b154-7abf-e063-6294a90ae6bb
Type HUMAN OTC DRUG
Nonproprietary name ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
Dosage form TABLET, EFFERVESCENT
Route ORAL
Labeler Select Consumer Group
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-03-02
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 Additional Listing Data#
Finished product Yes
Brand name base Alka-Seltzer Original
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANHYDROUS CITRIC ACID 1000 mg/1 ASPIRIN 325 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 XF417D3PSL Internal UNII lookup R16CO5Y76E Internal UNII lookup 8MDF5V39QO Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1536675 Internal RxNorm lookup 1536680 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 85237-1829-1 Alka-Seltzer Original 1 in 1 BLISTER PACK TABLET, EFFERVESCENT 1 1 85237-1829-1 Alka-Seltzer Original 2 in 1 POUCH TABLET, EFFERVESCENT 2 1
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 · 1,687 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 85237-1829-1 85237182901 1 POUCH in 1 BLISTER PACK (85237-1829-1) / 2 TABLET, EFFERVESCENT in 1 POUCH 1 pouch 2010-03-02 No No Current 85237-1829-2 85237182902 2 POUCH in 1 CONTAINER (85237-1829-2) / 2 TABLET, EFFERVESCENT in 1 POUCH (85237-1829-0) 2 pouch 2010-03-02 0 Current 85237-1829-3 85237182903 20 POUCH in 1 CARTON (85237-1829-3) / 2 TABLET, EFFERVESCENT in 1 POUCH (85237-1829-0) 20 pouch 2010-03-02 0 Current 85237-1829-4 85237182904 25 POUCH in 1 CARTON (85237-1829-4) / 2 TABLET, EFFERVESCENT in 1 POUCH (85237-1829-0) 25 pouch 2010-03-02 0 Current 85237-1829-6 85237182906 50 POUCH in 1 CARTON (85237-1829-6) / 2 TABLET, EFFERVESCENT in 1 POUCH (85237-1829-0) 50 pouch 2010-03-02 0 Current 85237-1829-7 85237182907 3 POUCH in 1 CONTAINER (85237-1829-7) / 2 TABLET, EFFERVESCENT in 1 POUCH (85237-1829-0) 3 pouch 2025-06-04 0 Current