NDC Package 79903-176-06 Multi-symptom Cold Childrens

Dextromethorphan Hbr,Guaifenesin,Phenylephrine Hcl Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
79903-176-06
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 201 mL in 1 BOTTLE, PLASTIC (79903-176-99)
Product Code:
Proprietary Name:
Multi-symptom Cold Childrens
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directeddo not take more than 6 doses in any 24-hour periodmL = milliliteronly use the dose cup provideddose as follows or as directed by a doctorAgeDosechildren 6 to under 12 years10 mL every 4 hourschildren 4 to under 6 years5 mL every 4 hourschildren under 4 yearsdo not use
11-Digit NDC Billing Format:
79903017606
NDC to 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
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walmart Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-09-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 79903-176-06?

    The NDC Packaged Code 79903-176-06 is assigned to a package of 1 bottle, plastic in 1 carton / 201 ml in 1 bottle, plastic (79903-176-99) of Multi-symptom Cold Childrens, a human over the counter drug labeled by Walmart Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 79903-176 included in the NDC Directory?

    Yes, Multi-symptom Cold Childrens with product code 79903-176 is active and included in the NDC Directory. The product was first marketed by Walmart Inc. on June 09, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 79903-176-06?

    The 11-digit format is 79903017606. 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 5-3-2 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
    5-3-279903-176-065-4-279903-0176-06