Mucinex Childrens Granule
NDC Package 72854-090-12

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

Package Information

Mucinex Childrens (acetaminophen and guaifenesin) granules is empty entire contents of packet onto tongue and swallowfor best taste, do not chew granulesAgeDoseadults and Children 12 years of age and over2 to 4 packets every 4 hours, not to exceed 6 doses (24 packets) in 24 hourschildren 6 years to under 12 years of age2 packets every 4 hours, not to exceed 5 doses (10 packets) in 24 hourschildren under 6 years of agedo not use. This formulation utilizes a granule delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 72854-090 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
72854-090-12
Package Description
12 PACKET in 1 CARTON / 1 GRANULE in 1 PACKET
Product Code
11-Digit Billing Format
72854009012
RxNorm Crosswalk
  • RxCUI: 2739993 - acetaminophen 162.5 MG / guaiFENesin 100 MG Oral Granules
  • RxCUI: 2739993 - acetaminophen 162.5 MG / guaifenesin 100 MG Oral Granules
  • RxCUI: 2739993 - APAP 162.5 MG / guaifenesin 100 MG Oral Granules

Clinical Specifications

Proprietary Name
Mucinex Childrens Mini Melts Cold And Flu
Non-Proprietary Name
Acetaminophen And Guaifenesin
Substance Name
Acetaminophen; Guaifenesin
Dosage Form
Granule - A small particle or grain.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Empty entire contents of packet onto tongue and swallowfor best taste, do not chew granulesAgeDoseadults and Children 12 years of age and over2 to 4 packets every 4 hours, not to exceed 6 doses (24 packets) in 24 hourschildren 6 years to under 12 years of age2 packets every 4 hours, not to exceed 5 doses (10 packets) in 24 hourschildren under 6 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
04-05-2026
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 72854-090-12 identifies a specific commercial package of 12 packet in 1 carton / 1 granule in 1 packet of Mucinex Childrens Mini Melts Cold And Flu, a human over the counter drug labeled by Reckitt Benckiser Llc. This granule is formulated for oral use and contains acetaminophen; guaifenesin 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 April 05, 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: 72854009012. 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)
72854-090-12
11-Digit CMS (5-4-2)
72854-0090-12

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