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  5. NDC Package Code: 71992-154-20 Alka Seltzer Plus Cold Day And Night Effervescent

NDC Package 71992-154-20 Alka Seltzer Plus Cold Day And Night Effervescent

Aspirin,Dextromethorphan Hydrobromide,Phenylephrine Bitartrate Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
71992-154-20
Package Description:
20 TABLET in 1 CARTON
Product Code:
71992-154
Proprietary Name:
Alka Seltzer Plus Cold Day And Night Effervescent
Non-Proprietary Name:
Aspirin, Dextromethorphan Hydrobromide, Phenylephrine Bitartrate
Substance Name:
Aspirin; Dextromethorphan Hydrobromide; Phenylephrine Bitartrate
Usage Information:
● adults and children 12 years and over: take 2 tablets fully dissolved in 4 oz of water at bedtime (may be taken every 4 to 6 hours). Do not exceed 8 tablets in 24 hours or as directed by a doctor. ● children under 12 years: do not use
11-Digit NDC Billing Format:
71992015420
NDC to RxNorm Crosswalk:
  • RxCUI: 1536498 - aspirin 325 MG / dextromethorphan HBr 10 MG / phenylephrine bitartrate 7.8 MG Effervescent Oral Tablet
  • RxCUI: 1536498 - aspirin 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine bitartrate 7.8 MG Effervescent Oral Tablet
  • RxCUI: 1536498 - ASA 325 MG / Dextromethorphan Hydrobromide 10 MG / Phenylephrine bitartrate 7.8 MG Effervescent Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Sincronia Logistica, S.a. De C.v.
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-02-2018
Listing Expiration Date:
12-31-2025
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 71992-154-20?

The NDC Packaged Code 71992-154-20 is assigned to a package of 20 tablet in 1 carton of Alka Seltzer Plus Cold Day And Night Effervescent, a human over the counter drug labeled by Sincronia Logistica, S.a. De C.v.. The product's dosage form is tablet and is administered via oral form.

Is NDC 71992-154 included in the NDC Directory?

Yes, Alka Seltzer Plus Cold Day And Night Effervescent with product code 71992-154 is active and included in the NDC Directory. The product was first marketed by Sincronia Logistica, S.a. De C.v. on July 02, 2018 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71992-154-20?

The 11-digit format is 71992015420. 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 5-3-2 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
5-3-271992-154-205-4-271992-0154-20