Mucinex Childrens Kit
NDC Package 72854-062-04
Package Information
Mucinex Childrens (acetaminophen, dextromethorphan hbr, triprolidine hcl) kits is day: Uses ■ 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 your child get to sleep ■ minor aches and pains ■ sore throat ■ headache ■ temporarily reduces fever Night: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 your child get to sleep. This formulation utilizes a kit delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 72854-062 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1919076 - acetaminophen 325 MG / dextromethorphan HBr 10 MG in 10 mL Oral Solution
- RxCUI: 1919076 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML Oral Solution
- RxCUI: 1919076 - acetaminophen 325 MG / dextromethorphan HBr 10 MG per 10 mL Oral Solution
- RxCUI: 1919076 - acetaminophen 650 MG / dextromethorphan HBr 20 MG per 20 mL Oral Solution
- RxCUI: 1919076 - APAP 32.5 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 72854 - Reckitt Benckiser Llc
- 72854-062 - Mucinex Childrens
- 72854-062-04 - 2 BOTTLE in 1 CARTON / 1 KIT in 1 BOTTLE * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE
- 72854-062 - Mucinex Childrens
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 72854-062-04 identifies a specific commercial package of 2 bottle in 1 carton / 1 kit in 1 bottle * 118 ml in 1 bottle * 118 ml in 1 bottle of Mucinex Childrens, a human over the counter drug labeled by Reckitt Benckiser Llc. This kit is formulated for oral 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 June 01, 2026. 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: 72854006204. 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.