Mucinex Nightshift Solution
NDC Package 63824-503-64
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
- 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
Regulatory & Marketing
Hierarchy Structure
- 63824 - Reckitt Benckiser Llc
- 63824-503 - Mucinex Nightshift
- 63824-503-64 - 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
- 63824-503 - Mucinex Nightshift
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.
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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.
* 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 63824-503-64 identifies a specific commercial package of 1 bottle in 1 carton / 118 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: 63824050364. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.