Mucus Relief Cold Flu And Sore Throat Liquid
NDC Package 63868-746-07

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

Package Information

Mucus Relief Cold Flu And Sore Throat (acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl) liquids is do not take more than directed (see Overdose warning)do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctormL=milliliteradults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hourschildren under 12 years of age: do not use. This formulation utilizes a liquid delivery system. Marketed by Quality Choice (chain Drug Marketing Association), this product is identified by NDC 63868-746 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
63868-746-07
Package Description
177 mL in 1 BOTTLE, PLASTIC
Product Code
63868-746
11-Digit Billing Format
63868074607
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
177 ML
RxNorm Crosswalk
  • RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1116572 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1116572 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG per 10 ML Oral Solution
  • RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine hydrochloride 10 MG per 20 ML Oral Solution
  • RxCUI: 1116572 - APAP 32.5 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Mucus Relief Cold Flu And Sore Throat Maximum Strength
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Substance Name
Acetaminophen; 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 directed (see Overdose warning)do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctormL=milliliteradults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hourschildren under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Quality Choice (chain Drug Marketing Association)
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-31-2015
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 63868-746-07 identifies a specific commercial package of 177 ml in 1 bottle, plastic of Mucus Relief Cold Flu And Sore Throat Maximum Strength, a human over the counter drug labeled by Quality Choice (chain Drug Marketing Association). This product is billed per "ML" milliliter and contains an estimated amount of 177 billable units per package. This liquid is formulated for oral use and contains acetaminophen; 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 Quality Choice (chain Drug Marketing Association) on January 31, 2015. The current certification is valid through December 31, 2026.

How is this Quality Choice (chain Drug Marketing Association) product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63868074607. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 177 total billable units per package. 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)
63868-746-07
11-Digit CMS (5-4-2)
63868-0746-07

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