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  5. NDC Package Code: 63824-269-66 Mucinex Nightshift Sinus

NDC Package 63824-269-66 Mucinex Nightshift Sinus

Acetaminophen,Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride,And Triprolidine - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
63824-269-66
Package Description:
180 mL in 1 BOTTLE
Product Code:
63824-269
Proprietary Name:
Mucinex Nightshift Sinus
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 Sinus-Max Severe Congestion & PainPurposesAcetaminophen 650mgPain relieverGuaifenesin 400 mgExpectorantPhenylephrine HCl 10 mgNasal decongestant Active ingredients (in each 20 mL)Mucinex Nightshift SinusPurposesAcetaminophen 650mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantPhenylephrine HCl 10 mgNasal decongestantTriprolidine HCl 2.5 mgAntihistamine
11-Digit NDC Billing Format:
63824026966
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
180 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 1116568 - acetaminophen 650 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1116568 - acetaminophen 32.5 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1116568 - acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution
  • RxCUI: 1116568 - acetaminophen 650 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1116568 - APAP 32.5 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/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.
    • Active Ingredient(s):
  • ACETAMINOPHEN 650 mg/20mL
  • DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL
  • PHENYLEPHRINE HYDROCHLORIDE 10 mg/20mL
  • TRIPROLIDINE HYDROCHLORIDE 2.5 mg/20mL
    • Pharmacologic Class(es):
  • Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
  • Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
  • Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • 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:
    06-15-2019
    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 63824-269-66?

    The NDC Packaged Code 63824-269-66 is assigned to a package of 180 ml in 1 bottle of Mucinex Nightshift Sinus, 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 63824-269 included in the NDC Directory?

    Yes, Mucinex Nightshift Sinus with product code 63824-269 is active and included in the NDC Directory. The product was first marketed by Rb Health (us) Llc on June 15, 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 NDC billing unit for package 63824-269-66?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 180.

    What is the 11-digit format for NDC 63824-269-66?

    The 11-digit format is 63824026966. 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
    5-3-263824-269-665-4-263824-0269-66