Mucinex Childrens Day Time Multi-symptom Cold And Mucinex Childrens Night Time Multi-symptom Cold Triple Pack Kit
NDC Package 63824-944-34

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Mucinex Childrens Day Time Multi-symptom Cold And Mucinex Childrens Night Time Multi-symptom Cold Triple Pack (acetaminophen, diphenylhydramine hydrochloride, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin) kits is this product does not contain directions or complete warnings for adult usedo not give more than directed (see Overdose warning)measure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorchildren 6 to under 12 years of age: 10 mL in dosing cup provided every 4 hours while symptoms last; do not give more than 5 doses in any 24-hour periodchildren under 6 years of age: do not use do not give more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorAgeDosechildren 6 to under 12 years of age10 mL every 4 hourschildren 4 to under 6 years of age5 mL every 4 hourschildren under 4 years of agedo not use. This formulation utilizes a kit delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 63824-944 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
63824-944-34
Package Description
1 KIT in 1 CARTON * 1 BOTTLE in 1 CARTON (63824-949-01) / 118 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (63824-950-21) / 118 mL in 1 BOTTLE
Product Code
63824-944
11-Digit Billing Format
63824094434
RxNorm Crosswalk
  • RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution
  • RxCUI: 1043543 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1043543 - dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution
  • RxCUI: 1375932 - acetaminophen 650 MG / diphenhydrAMINE HCl 25 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution

Clinical Specifications

Proprietary Name
Mucinex Childrens Day Time Multi-symptom Cold And Mucinex Childrens Night Time Multi-symptom Cold Triple Pack
Non-Proprietary Name
Acetaminophen, Diphenylhydramine Hydrochloride, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, And Guaifenesin
Dosage Form
Kit - A packaged collection of related material.
Usage Information
This product does not contain directions or complete warnings for adult usedo not give more than directed (see Overdose warning)measure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorchildren 6 to under 12 years of age: 10 mL in dosing cup provided every 4 hours while symptoms last; do not give more than 5 doses in any 24-hour periodchildren under 6 years of age: do not use do not give more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorAgeDosechildren 6 to under 12 years of age10 mL every 4 hourschildren 4 to under 6 years of age5 mL every 4 hourschildren under 4 years of agedo not use

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-25-2022
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 63824-944-34 identifies a specific commercial package of 1 kit in 1 carton * 1 bottle in 1 carton (63824-949-01) / 118 ml in 1 bottle * 1 bottle in 1 carton (63824-950-21) / 118 ml in 1 bottle of Mucinex Childrens Day Time Multi-symptom Cold And Mucinex Childrens Night Time Multi-symptom Cold Triple Pack, a human over the counter drug labeled by Reckitt Benckiser Llc. This kit is formulated for use and contains 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 May 25, 2022. 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: 63824094434. 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)
63824-944-34
11-Digit CMS (5-4-2)
63824-0944-34

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