Home NDC 70264-014 Alka-Seltzer Original
Product NDC 70264-014
11-digit product format 702640014
Labeler code 70264
Product ID 70264-014_43c89573-4cf2-997f-e063-6394a90a76ca
Type HUMAN OTC DRUG
Nonproprietary name ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
Dosage form TABLET, EFFERVESCENT
Route ORAL
Labeler R J General Corporation
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 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 70264-014-01 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 70264-014-01 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 70264-014-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 70264-014-01 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 70264-014-01 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 70264-014-01 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base Alka-Seltzer Original
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 1000 mg/1 SODIUM BICARBONATE 325 mg/1 ANHYDROUS CITRIC ACID 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 8MDF5V39QO Internal UNII lookup XF417D3PSL 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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70264-014-01 Alka-Seltzer Original 2 in 1 POUCH TABLET, EFFERVESCENT 2 6 70264-014-01 Alka-Seltzer Original 50 in 1 CARTON TABLET, EFFERVESCENT 50 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70264-014 ALKA-SELTZER ORIGINAL (ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE) TABLET, EFFERVESCENT [R J GENERAL CORPORATION] 5 Current NDC, Legacy NDC, 2 package rows 20241030_dbb0d067-71f0-45e4-bc98-548cf4a90b3a.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 84 · 1,678 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 70264-014-01 70264001401 50 POUCH in 1 CARTON (70264-014-01) / 2 TABLET, EFFERVESCENT in 1 POUCH 50 pouch 2010-03-02 0000-00-00 No No Current