NDC Package 63824-504-66 Mucinex Nightshift Severe Cold And Flu

Acetaminophen,Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride,And Triprolidine - 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:
63824-504-66
Package Description:
180 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Mucinex Nightshift Severe Cold And Flu
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, And Triprolidine Hydrochloride
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride; Triprolidine Hydrochloride
Usage Information:
This product is used as Active ingredients (in each 20 mL)MUCINEX FAST-MAX COLD & FLUPurposesAcetaminophen 650 mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantGuaifenesin 400 mgExpectorantPhenylephrine HCl 10 mgNasal decongestantActive ingredients (in each 20 mL) MUCINEX NIGHTSHIFT SEVERE COLD & FLUPurposesAcetaminophen 650 mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantPhenylephrine HCl 10 mgNasal decongestantTriprolidine HCl 2.5 mgAntihistamine
11-Digit NDC Billing Format:
63824050466
Product Type:
Human Otc Drug
Labeler Name:
Rb Health (us) Llc
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:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-01-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 63824-504-66?

    The NDC Packaged Code 63824-504-66 is assigned to a package of 180 ml in 1 bottle of Mucinex Nightshift Severe Cold And Flu, a human over the counter drug labeled by Rb Health (us) Llc. The product's dosage form is solution and is administered via oral form.

    Is NDC 63824-504 included in the NDC Directory?

    Yes, Mucinex Nightshift Severe Cold And Flu with product code 63824-504 is active and included in the NDC Directory. The product was first marketed by Rb Health (us) Llc on June 01, 2020 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 63824-504-66?

    The 11-digit format is 63824050466. 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
    5-3-263824-504-665-4-263824-0504-66