Tussin Cf Multi-symptom Cold Liquid
NDC Package 53942-504-26

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

Package Information

Tussin Cf Multi-symptom Cold (dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride) liquids is do not take more than 6 doses in any 24 hour periodThis adult strength product is not intended for use in children under 12 years of ageAge                                                                               Doseadults and children 12 years and over                               2 teaspoons every 4 hours children under 12                                                           do not use. This formulation utilizes a liquid delivery system. Marketed by Demoulas Market Basket, this product is identified by NDC 53942-504 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
53942-504-26
Package Description
237 mL in 1 BOTTLE
Product Code
53942-504
11-Digit Billing Format
53942050426
RxNorm Crosswalk
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 10 mL Oral Solution
  • RxCUI: 1044949 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 10 MG / guaifenesin 100 MG / phenylephrine HCl 5 MG per 5 ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 MG per 10 ML Oral Solution

Clinical Specifications

Proprietary Name
Tussin Cf Multi-symptom Cold
Non-Proprietary Name
Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
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 periodThis adult strength product is not intended for use in children under 12 years of ageAge                                                                               Doseadults and children 12 years and over                               2 teaspoons every 4 hours children under 12                                                           do not use

Regulatory & Marketing

Labeler Name
Demoulas Market Basket
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-20-2012
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 53942-504-26 identifies a specific commercial package of 237 ml in 1 bottle of Tussin Cf Multi-symptom Cold, a human over the counter drug labeled by Demoulas Market Basket. This liquid is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin; phenylephrine 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 Demoulas Market Basket on September 20, 2012. The current certification is valid through December 31, 2026.

How is this Demoulas Market Basket product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53942050426. 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)
53942-504-26
11-Digit CMS (5-4-2)
53942-0504-26

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