Next Day Time
NDC Package 50066-356-09

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.

Next Day Time is ■ do not take more than directed (see Warnings)Adults and children 12 years and over: ■ take 2 caplets every 4 hours ■ do not take more than a total of 12 caplets in 24 hoursChildren under 12 years:Do not use this adult product in children under 12 years of age. Marketed by Genomma Lab Usa, this product is identified by NDC 50066-356 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
50066-356-09
Package Description
10 CAPSULE, LIQUID FILLED in 1 BOX
Product Code
50066-356
11-Digit Billing Format
50066035609
RxNorm Crosswalk
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
Next Day Time Non Drowsy Cold And Flue
Dosage Form
-
Usage Information
■ do not take more than directed (see Warnings)Adults and children 12 years and over: ■ take 2 caplets every 4 hours ■ do not take more than a total of 12 caplets in 24 hoursChildren under 12 years:Do not use this adult product in children under 12 years of age. This will provide more than the recommended dose (overdose) and may cause liver damage.

Regulatory & Marketing

Labeler Name
Genomma Lab Usa
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-19-2015
Listing Expiration
12-31-2017
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 50066-356-09 identifies a specific commercial package of 10 capsule, liquid filled in 1 box of Next Day Time Non Drowsy Cold And Flue, labeled by Genomma Lab Usa. 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 Genomma Lab Usa on January 19, 2015. The current certification is valid through December 31, 2017.

How is this Genomma Lab Usa product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50066035609. 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)
50066-356-09
11-Digit CMS (5-4-2)
50066-0356-09

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