NDC Package 66715-5106-0 Alka-seltzer

Aspirin,Citric Acid,Sodium Bicarbonate Effervescent Tablet Tablet, Effervescent Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
66715-5106-0
Package Description:
15 POUCH in 1 BOX, UNIT-DOSE / 2 TABLET, EFFERVESCENT in 1 POUCH
Product Code:
Proprietary Name:
Alka-seltzer
Non-Proprietary Name:
Aspirin, Citric Acid, Sodium Bicarbonate Effervescent Tablet
Substance Name:
Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate
Usage Information:
Fully dissolve 2 tablets in 4 ounces of water before taking.Adults and children 12 years and over: take 2 tablets every 4 hours,or as directed by a doctor. Do not exceed 8 tablets in 24 hours. Adults 60 years and over: take 2 tablets every 4 hours,or as directed by a doctor. Do not exceed 4 tablets in 24 hours. Children under 12 years: consult a doctor.
11-Digit NDC Billing Format:
66715510600
NDC to 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
Product Type:
Human Otc Drug
Labeler Name:
Lil' Drug Store Products, Inc.
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(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
M001
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-17-2008
End Marketing Date:
06-01-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 66715-5106-0?

The NDC Packaged Code 66715-5106-0 is assigned to a package of 15 pouch in 1 box, unit-dose / 2 tablet, effervescent in 1 pouch of Alka-seltzer, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet, effervescent and is administered via oral form.

Is NDC 66715-5106 included in the NDC Directory?

Yes, Alka-seltzer with product code 66715-5106 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on January 17, 2008.

What is the 11-digit format for NDC 66715-5106-0?

The 11-digit format is 66715510600. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-166715-5106-05-4-266715-5106-00