1. Home
  2. Labeler Index
  3. Chain Drug Manufacturing Assn
  4. 63868-290
  5. NDC Package Code: 63868-290-06 Severe Cold And Cough Daytime

NDC Package 63868-290-06 Severe Cold And Cough Daytime

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
63868-290-06
Package Description:
6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET
Product Code:
63868-290
Proprietary Name:
Severe Cold And Cough Daytime
Usage Information:
•do not use more than directed•take every 4 hours; while symptoms persist. Do not to exceed 5 packets in 24 hours unless directed by a doctorAgeDoseAdults and children 12 years of age and overOne packetChildren under 12 years of ageDo not use•dissolve contents of one packet into 8 oz hot water; sip while hot. Consume entire drink within 10-15 minutes•If using a microwave, add contents of one packet 8 oz. of cool water: Stir briskly before and after heating: Do not overheat.
11-Digit NDC Billing Format:
63868029006
NDC to RxNorm Crosswalk:
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Powder for Oral Solution
  • RxCUI: 1659967 - APAP 650 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution
    • Labeler Name:
    Chain Drug Manufacturing Assn
    Sample Package:
    No
    Start Marketing Date:
    07-25-2018
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 63868-290-06?

    The NDC Packaged Code 63868-290-06 is assigned to a package of 6 packet in 1 carton / 1 powder, for solution in 1 packet of Severe Cold And Cough Daytime, labeled by Chain Drug Manufacturing Assn. The product's dosage form is and is administered via form.

    Is NDC 63868-290 included in the NDC Directory?

    No, Severe Cold And Cough Daytime with product code 63868-290 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Chain Drug Manufacturing Assn on July 25, 2018 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 63868-290-06?

    The 11-digit format is 63868029006. 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
    5-3-263868-290-065-4-263868-0290-06