Mucinex Nightshift Solution
NDC Package 63824-503-69

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Mucinex Nightshift (acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride) solution is a medication used as Active ingredients (in each 20 mL) MUCINEX FAST-MAX DM MAX PurposesDextromethorphan HBr 20 mgCough suppressantGuaifenesin 400 mgExpectorantActive ingredients (in each 20 mL) MUCINEX NIGHTTIME COLD & FLU PurposesAcetaminophen 650 mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantTriprolidine HCl 2.5 mgAntihistamine. This formulation utilizes a solution delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 63824-503 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
63824-503-69
Package Description
266 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
63824050369
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
266 ML
RxNorm Crosswalk
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
  • RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 2173667 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / triprolidine HCl 2.5 MG in 20 mL Oral Solution

Clinical Specifications

Proprietary Name
Mucinex Nightshift Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, And Triprolidine Hydrochloride
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Triprolidine Hydrochloride
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
This product is used as Active ingredients (in each 20 mL) MUCINEX FAST-MAX DM MAX PurposesDextromethorphan HBr 20 mgCough suppressantGuaifenesin 400 mgExpectorantActive ingredients (in each 20 mL) MUCINEX NIGHTTIME COLD & FLU PurposesAcetaminophen 650 mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantTriprolidine HCl 2.5 mgAntihistamine. Helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-15-2019
Listing Expiration
12-31-2027
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 (63824-503). Click a package code to view its specific billing and regulatory data.

1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
180 mL in 1 BOTTLE

* 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 63824-503-69 identifies a specific commercial package of 266 ml in 1 bottle of Mucinex Nightshift Cold And Flu, a human over the counter drug labeled by Reckitt Benckiser Llc. This solution is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; triprolidine hydrochloride 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 Reckitt Benckiser Llc on June 15, 2019. The current certification is valid through December 31, 2027.

How is this Reckitt Benckiser Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63824050369. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 266 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 (5-3-2)
63824-503-69
11-Digit CMS (5-4-2)
63824-0503-69

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