NDC Package 0363-7550-04 Walgreens Daytime Childrens

Cough And Chest Congestion Liquid 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:
0363-7550-04
Package Description:
118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Walgreens Daytime Childrens
Non-Proprietary Name:
Cough And Chest Congestion
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
▪measure only with dosing cup provided.▪keep dosing cup with product ▪mL= milliliter ▪do not take more than 6 doses in any 24-hour periodagedoseChildren under 4 yearsDo not useChildren 4 to under 6 years5 mL every 4 hoursChildren 6 to under 12 years10 mL every 4 hoursAdults and children 12 years and older20 mL every 4 hours
11-Digit NDC Billing Format:
00363755004
NDC to RxNorm Crosswalk:
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
  • RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walgreens Co.
    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(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:
    07-16-2019
    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 0363-7550-04?

    The NDC Packaged Code 0363-7550-04 is assigned to a package of 118 ml in 1 bottle of Walgreens Daytime Childrens, a human over the counter drug labeled by Walgreens Co.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 0363-7550 included in the NDC Directory?

    Yes, Walgreens Daytime Childrens with product code 0363-7550 is active and included in the NDC Directory. The product was first marketed by Walgreens Co. on July 16, 2019 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 0363-7550-04?

    The 11-digit format is 00363755004. 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
    4-4-20363-7550-045-4-200363-7550-04