Alka-seltzer Original Tablet, Effervescent
NDC Package 0280-4000-07

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Alka-seltzer Original (anhydrous citric acid, aspirin, and sodium bicarbonate) tablets is directions● fully dissolve 2 tablets in 4 ounces of water before takingadults and children 12 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 8 tablets in 24 hoursadults 60 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 4 tablets in 24 hourschildren under 12 yearsconsult a doctor. This formulation utilizes a tablet, effervescent delivery system. Marketed by Bayer Healthcare Llc., this product is identified by NDC 0280-4000 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
0280-4000-07
Package Description
26 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
Product Code
0280-4000
11-Digit Billing Format
00280400007
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
26 EA
RxNorm Crosswalk
  • RxCUI: 1536675 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536675 - ASA 325 MG / Citric Acid 1000 MG / NaHCO3 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536680 - Alka-Seltzer 325 MG / 1000 MG / 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536680 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet [Alka-Seltzer]
  • RxCUI: 1536680 - Alka-Seltzer (aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG) Effervescent Oral Tablet

Clinical Specifications

Proprietary Name
Alka-seltzer Original
Non-Proprietary Name
Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate
Substance Name
Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate
Dosage Form
Tablet, Effervescent - A solid dosage form containing mixtures of acids (e.g., citric acid, tartaric acid) and sodium bicarbonate, which release carbon dioxide when dissolved in water; it is intended to be dissolved or dispersed in water before administration.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Directions● fully dissolve 2 tablets in 4 ounces of water before takingadults and children 12 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 8 tablets in 24 hoursadults 60 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 4 tablets in 24 hourschildren under 12 yearsconsult a doctor

Regulatory & Marketing

Labeler Name
Bayer Healthcare Llc.
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-02-2010
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0280-4000). Click a package code to view its specific billing and regulatory data.

0280-4000-01
6 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
0280-4000-02
24 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
0280-4000-03
18 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
0280-4000-04
58 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
0280-4000-05
36 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
0280-4000-06
12 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0280-4000-07 identifies a specific commercial package of 26 pouch in 1 carton / 2 tablet, effervescent in 1 pouch of Alka-seltzer Original, a human over the counter drug labeled by Bayer Healthcare Llc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 26 billable units per package. This tablet, effervescent is formulated for oral use and contains anhydrous citric acid; aspirin; sodium bicarbonate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bayer Healthcare Llc. on March 02, 2010. The current certification is valid through December 31, 2026.

How is this Bayer Healthcare Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00280400007. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 26 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0280-4000-07
11-Digit CMS (5-4-2)
00280-4000-07

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.