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  5. NDC Package Code: 0067-6094-01 Theraflu Powerpods Daytime Severe Cold

NDC Package 0067-6094-01 Theraflu Powerpods Daytime Severe Cold

Acetaminophen,Dextromethorphan,Phenylephrine Powder, For Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
0067-6094-01
Package Description:
8 POUCH in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 POUCH (0067-6094-02)
Product Code:
0067-6094
Proprietary Name:
Theraflu Powerpods Daytime Severe Cold
Non-Proprietary Name:
Acetaminophen, Dextromethorphan, Phenylephrine
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
•do not use more than directed•take every 4 hours, while symptoms persist. Do not take more than 5 pods in 24 hours unless directed by a doctor.AgeDoseadults and children 12 years of age and overone podchildren under 12 years of agedo not use•do not remove the foil seal as the pod will not work properly and could result in hot water burns •place pod in compatible brewer•use a minimum of 8 oz. of water •when finished, the pod will be hot and may drip. Tilt the pod during removal to avoid dripping. •remove used pod and flush brewer after use with a minimum of 8 oz. of water•sip while hot. Consume entire drink within 10-15 minutes.
11-Digit NDC Billing Format:
00067609401
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
8 EA
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
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Haleon Us Holdings Llc
    Dosage Form:
    Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 650 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE 20 mg/1
  • PHENYLEPHRINE HYDROCHLORIDE 10 mg/1
    • 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:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-28-2018
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0067-6094-031 POUCH in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0067-6094-01?

    The NDC Packaged Code 0067-6094-01 is assigned to a package of 8 pouch in 1 carton / 1 powder, for solution in 1 pouch (0067-6094-02) of Theraflu Powerpods Daytime Severe Cold, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is powder, for solution and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 8 billable units per package.

    Is NDC 0067-6094 included in the NDC Directory?

    Yes, Theraflu Powerpods Daytime Severe Cold with product code 0067-6094 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on July 28, 2018 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0067-6094-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 8.

    What is the 11-digit format for NDC 0067-6094-01?

    The 11-digit format is 00067609401. 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
    4-4-20067-6094-015-4-200067-6094-01