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  5. NDC Package Code: 0031-8729-01 Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride

NDC Package 0031-8729-01 Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride

Syrup - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0031-8729-01
Package Description:
75708 mL in 1 CONTAINER
Product Code:
0031-8729
Non-Proprietary Name:
Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
11-Digit NDC Billing Format:
00031872901
Product Type:
Bulk Ingredient
Labeler Name:
Haleon Us Holdings Llc
Dosage Form:
Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
Active Ingredient(s):
  • DEXTROMETHORPHAN HYDROBROMIDE 10 mg/5mL
  • GUAIFENESIN 100 mg/5mL
  • PHENYLEPHRINE HYDROCHLORIDE 5 mg/5mL
    • Sample Package:
    N/A
    Marketing Category:
    EXPORT ONLY - A product that is only exported and not marketed in the United States.
    Start Marketing Date:
    09-01-2015
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    Code 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 disclaimer below.

    Frequently Asked Questions

    What is NDC 0031-8729-01?

    The NDC Packaged Code 0031-8729-01 is assigned to an UNFINISHED drug package of 75708 ml in 1 container of Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, a bulk ingredient labeled by Haleon Us Holdings Llc. The product's dosage form is syrup and is administered via form.

    Is NDC 0031-8729 included in the NDC Directory?

    Yes, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride is an UNFINISHED PRODUCT with code 0031-8729 that is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on September 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0031-8729-01?

    The 11-digit format is 00031872901. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    4-4-20031-8729-015-4-200031-8729-01