Onessip Adult Daytime Severe Cold And Flu Solution
NDC Package 87078-972-32

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Onessip Adult Daytime Severe Cold And Flu (acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci) solution is usestemporarily relieves common cold/flu symptoms: nasal congestionsinus congestion & pressurecough due to minor throat & bronchial irritationminor aches & painsheadachefeversore throatreduces swelling of nasal passagestemporarily restores freer breathing through the nosepromotes nasal and/or sinus drainagehelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive. This formulation utilizes a solution delivery system. Marketed by Medwise Lifesciences Inc., this product is identified by NDC 87078-972 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
87078-972-32
Package Description
12 POUCH in 1 CARTON / 15 mL in 1 POUCH (87078-972-03)
Product Code
87078-972
11-Digit Billing Format
87078097232

Clinical Specifications

Proprietary Name
Onessip Adult Daytime Severe Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hci
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Usestemporarily relieves common cold/flu symptoms: nasal congestionsinus congestion & pressurecough due to minor throat & bronchial irritationminor aches & painsheadachefeversore throatreduces swelling of nasal passagestemporarily restores freer breathing through the nosepromotes nasal and/or sinus drainagehelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive.

Regulatory & Marketing

Labeler Name
Medwise Lifesciences Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-15-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 87078-972-32 identifies a specific commercial package of 12 pouch in 1 carton / 15 ml in 1 pouch (87078-972-03) of Onessip Adult Daytime Severe Cold And Flu, a human over the counter drug labeled by Medwise Lifesciences Inc.. This solution is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; guaifenesin; phenylephrine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Medwise Lifesciences Inc. on December 15, 2025. The current certification is valid through December 31, 2026.

How is this Medwise Lifesciences Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87078097232. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
87078-972-32
11-Digit CMS (5-4-2)
87078-0972-32

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.