Kids Cough Daytime Nighttime Combo
NDC Package 69676-0090-9

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Kids Cough Daytime Nighttime Combo is uses • temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive Uses • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat. Marketed by Genexa Inc., this product is identified by NDC 69676-0090 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
69676-0090-9
Package Description
1 BOTTLE in 1 KIT / 1 KIT in 1 BOTTLE * 118 mL in 1 BOTTLE, PLASTIC * 118 mL in 1 BOTTLE
Product Code
69676-0090
11-Digit Billing Format
69676009009
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
  • RxCUI: 1111440 - chlorpheniramine maleate 1 MG / dextromethorphan HBr 7.5 MG in 5 mL Oral Solution

Clinical Specifications

Proprietary Name
Kids Cough Daytime Nighttime Combo
Dosage Form
-
Usage Information
Uses • temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive Uses • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat

Regulatory & Marketing

Labeler Name
Genexa Inc.
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-26-2024
Listing Expiration
12-31-2025
Exclude Flag
I
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 69676-0090-9 identifies a specific commercial package of 1 bottle in 1 kit / 1 kit in 1 bottle * 118 ml in 1 bottle, plastic * 118 ml in 1 bottle of Kids Cough Daytime Nighttime Combo, labeled by Genexa Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Genexa Inc. on January 26, 2024. The current certification is valid through December 31, 2025.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69676009009. 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)
69676-0090-9
11-Digit CMS (5-4-2)
69676-0090-09

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