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  5. NDC Package Code: 72854-209-20 Mucinex Nightshift Sinus Maximum Strength

NDC Package 72854-209-20 Mucinex Nightshift Sinus Maximum Strength

Acetaminophen,Dextromethorphan Hydrobromide,And Triprolidine Hydrochloride Tablet, Coated - 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:
72854-209-20
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET, COATED in 1 BLISTER PACK
Product Code:
72854-209
Proprietary Name:
Mucinex Nightshift Sinus Maximum Strength
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, And Triprolidine Hydrochloride
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Triprolidine Hydrochloride
Usage Information:
Uses ■ temporarily relieves these common cold and flu symptoms: ■ cough ■ minor aches and pains ■ sore throat ■ headache ■ runny nose ■ sneezing ■ itching of the nose or throat ■ itchy, watery eyes due to hay fever ■ temporarily reduces fever ■ controls cough to help you get to sleep
11-Digit NDC Billing Format:
72854020920
NDC to RxNorm Crosswalk:
  • RxCUI: 2549034 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet
  • RxCUI: 2549034 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Rb Health (us) Llc
Dosage Form:
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
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:
05-01-2025
Listing Expiration Date:
12-31-2026
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 72854-209-20?

The NDC Packaged Code 72854-209-20 is assigned to a package of 2 blister pack in 1 carton / 10 tablet, coated in 1 blister pack of Mucinex Nightshift Sinus Maximum Strength, a human over the counter drug labeled by Rb Health (us) Llc. The product's dosage form is tablet, coated and is administered via oral form.

Is NDC 72854-209 included in the NDC Directory?

Yes, Mucinex Nightshift Sinus Maximum Strength with product code 72854-209 is active and included in the NDC Directory. The product was first marketed by Rb Health (us) Llc on May 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72854-209-20?

The 11-digit format is 72854020920. 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
5-3-272854-209-205-4-272854-0209-20