Home NDC 0280-0211 Alka-Seltzer Extra Strength
Product NDC 0280-0211
11-digit product format 002800211
Labeler code 0280
Product ID 0280-0211_45266611-610c-a481-e063-6394a90a1bf0
Type HUMAN OTC DRUG
Nonproprietary name Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin
Dosage form GRANULE, EFFERVESCENT
Route ORAL
Labeler Bayer HealthCare LLC.
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-04-11
Substance ANHYDROUS CITRIC ACID; SODIUM BICARBONATE; ASPIRIN
Active strength 1000; 1985; 500 mg/1; mg/1; mg/1
Pharmacologic classes Acidifying 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], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Platelet Aggregation Inhibitor [EPC]
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 Alka-Seltzer Extra Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANHYDROUS CITRIC ACID 1000 mg/1 SODIUM BICARBONATE 1985 mg/1 ASPIRIN 500 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 8MDF5V39QO Internal UNII lookup R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1872085 Internal RxNorm lookup 1872088 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 0280-0211-24 Alka-Seltzer Extra Strength 12 in 1 CARTON GRANULE, EFFERVESCENT 12 5 0280-0211-24 Alka-Seltzer Extra Strength 2 in 1 PACKET GRANULE, EFFERVESCENT 2 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0280-0211 ALKA-SELTZER EXTRA STRENGTH (ANHYDROUS CITRIC ACID, SODIUM BICARBONATE, AND ASPIRIN) GRANULE, EFFERVESCENT [BAYER HEALTHCARE LLC.] 4 Current NDC, Legacy NDC, 2 package rows 20231205_49b73bd5-6465-05eb-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 8 of 34 · 678 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 0280-0211-24 00280021124 12 PACKET in 1 CARTON (0280-0211-24) / 2 GRANULE, EFFERVESCENT in 1 PACKET 12 packet 2011-04-18 0000-00-00 No No Current