Daytime Severe Cold And Flu Suspension
NDC Package 69676-0093-9

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

Package Information

Daytime Severe Cold And Flu (acetaminophen, dextromethorphan hbr) suspension is usestemporarily reduces fever and relieves these common cold/flu symptoms:minor aches and painsheadachesore throatcough due to minor throat and bronchial irritationcontrols the impulse to cough to help you get to sleep Usestemporarily relieves these common cold and flu symptoms:cough due to minor throat and bronchial irritationminor aches and painssore throatheadacherunny nosesneezingtemporarily reduces fevercontrols cough to help you get to sleep. This formulation utilizes a suspension delivery system. Marketed by Genexa Inc., this product is identified by NDC 69676-0093 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
69676-0093-9
Package Description
177 mL in 1 BOTTLE
Product Code
69676-0093
11-Digit Billing Format
69676009309
RxNorm Crosswalk
  • RxCUI: 2692302 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 20 mL Oral Suspension
  • RxCUI: 2692302 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML / doxylamine succinate 0.625 MG/ML Oral Suspension
  • RxCUI: 2692302 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG per 20 ML Oral Suspension
  • RxCUI: 2692302 - APAP 32.5 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML / doxylamine succinate 0.625 MG/ML Oral Suspension
  • RxCUI: 2693772 - acetaminophen 650 MG / dextromethorphan HBr 20 MG in 20 mL Oral Suspension

Clinical Specifications

Proprietary Name
Daytime Severe Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide
Dosage Form
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Usestemporarily reduces fever and relieves these common cold/flu symptoms:minor aches and painsheadachesore throatcough due to minor throat and bronchial irritationcontrols the impulse to cough to help you get to sleep Usestemporarily relieves these common cold and flu symptoms:cough due to minor throat and bronchial irritationminor aches and painssore throatheadacherunny nosesneezingtemporarily reduces fevercontrols cough to help you get to sleep

Regulatory & Marketing

Labeler Name
Genexa Inc.
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-03-2024
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 69676-0093-9 identifies a specific commercial package of 177 ml in 1 bottle of Daytime Severe Cold And Flu, a human over the counter drug labeled by Genexa Inc.. This suspension is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide 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 Genexa Inc. on July 03, 2024. The current certification is valid through December 31, 2026.

How is this Genexa Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69676009309. 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 (5-4-1)
69676-0093-9
11-Digit CMS (5-4-2)
69676-0093-09

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