NDC Package 63824-535-66 Mucinex Fast-max Dm Max Honey And Berry Flavor

Dextromethorphan Hydrobromide And Guaifenesin 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:
63824-535-66
Package Description:
180 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Mucinex Fast-max Dm Max Honey And Berry Flavor
Non-Proprietary Name:
Dextromethorphan Hydrobromide And Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctoradults and children 12 years of age and over: 20 mL in dosing cup provided every 4 hourschildren under 12 years of age: do not use
11-Digit NDC Billing Format:
63824053566
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:
    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 63824-535-66?

    The NDC Packaged Code 63824-535-66 is assigned to a package of 180 ml in 1 bottle of Mucinex Fast-max Dm Max Honey And Berry Flavor, 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 63824-535 included in the NDC Directory?

    Yes, Mucinex Fast-max Dm Max Honey And Berry Flavor with product code 63824-535 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 63824-535-66?

    The 11-digit format is 63824053566. 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
    5-3-263824-535-665-4-263824-0535-66