Maximum Strength Mucus Relief Severe Congestion And Cough Liquid
NDC Package 49035-976-06

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

Package Information

Maximum Strength Mucus Relief Severe Congestion And Cough (dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride) liquids is •do not take more than 6 doses in any 24-hour period•measure only with dosing cup provided•do not use dosing cup with other products•dose as follows or as directed by a doctor•mL = milliliter•adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours.•children under 12 years of age: Do not use. This formulation utilizes a liquid delivery system. Marketed by Wal-mart Stores,inc.,, this product is identified by NDC 49035-976 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
49035-976-06
Package Description
180 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
49035097606
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

Clinical Specifications

Proprietary Name
Maximum Strength Mucus Relief Severe Congestion And Cough
Non-Proprietary Name
Dextromethorphan Hydrobromide, Guaifenesin, And 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.
Usage Information
•do not take more than 6 doses in any 24-hour period•measure only with dosing cup provided•do not use dosing cup with other products•dose as follows or as directed by a doctor•mL = milliliter•adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours.•children under 12 years of age: Do not use.

Regulatory & Marketing

Labeler Name
Wal-mart Stores,inc.,
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-02-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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 49035-976-06 identifies a specific commercial package of 180 ml in 1 bottle, plastic of Maximum Strength Mucus Relief Severe Congestion And Cough, a human over the counter drug labeled by Wal-mart Stores,inc.,. 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 Wal-mart Stores,inc., on May 02, 2018. The current certification is valid through December 31, 2026.

How is this Wal-mart Stores,inc., product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49035097606. 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)
49035-976-06
11-Digit CMS (5-4-2)
49035-0976-06

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