Childrens Robitussin Cough And Chest Congestion Dm Liquid
NDC Package 0031-8702-13

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

Package Information

Childrens Robitussin Cough And Chest Congestion Dm (dextromethorphan hydrobromide and guaifenesin) liquids is do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup providedkeep dosing cup with productmL = milliliteragedosechildren under 4 yearsdo not usechildren 4 to under 6 years5 mL every 4 hourschildren 6 to under 12 years10 mL every 4 hoursadults and children 12 years and over20 mL every 4 hours. This formulation utilizes a liquid delivery system. Marketed by Haleon Us Holdings Llc, this product is identified by NDC 0031-8702 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
0031-8702-13
Package Description
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code
0031-8702
11-Digit Billing Format
00031870213
RxNorm Crosswalk
  • RxCUI: 1111440 - chlorpheniramine maleate 1 MG / dextromethorphan HBr 7.5 MG in 5 mL Oral Solution
  • RxCUI: 1111440 - chlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML Oral Solution
  • RxCUI: 1111440 - chlorpheniramine maleate 1 MG / dextromethorphan hydrobromide 7.5 MG per 5 ML Oral Solution
  • RxCUI: 1111440 - chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG per 10 ML Oral Solution
  • RxCUI: 1790650 - dextromethorphan HBr 10 MG / guaiFENesin 100 MG in 10 mL Oral Solution

Clinical Specifications

Proprietary Name
Childrens Robitussin Cough And Chest Congestion Dm
Non-Proprietary Name
Dextromethorphan Hydrobromide And Guaifenesin
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup providedkeep dosing cup with productmL = milliliteragedosechildren under 4 yearsdo not usechildren 4 to under 6 years5 mL every 4 hourschildren 6 to under 12 years10 mL every 4 hoursadults and children 12 years and over20 mL every 4 hours

Regulatory & Marketing

Labeler Name
Haleon Us Holdings Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-12-2020
Listing Expiration
12-31-2026
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 0031-8702-13 identifies a specific commercial package of 1 bottle in 1 carton / 118 ml in 1 bottle of Childrens Robitussin Cough And Chest Congestion Dm, a human over the counter drug labeled by Haleon Us Holdings Llc. This liquid is formulated for oral use and contains dextromethorphan hydrobromide; 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 Haleon Us Holdings Llc on May 12, 2020. The current certification is valid through December 31, 2026.

How is this Haleon Us Holdings Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00031870213. 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 (4-4-2)
0031-8702-13
11-Digit CMS (5-4-2)
00031-8702-13

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