Conrx Cold
NDC Package 68737-232-16

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.

Conrx Cold is • do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets every 4 hours swallow whole - do not crush, chew or dissolvedo not take more than 12 caplets in 24 hourschildren under 12 yearsdo 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. Marketed by Eagle Distributors,inc., this product is identified by NDC 68737-232 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
68737-232-16
Package Description
50 POUCH in 1 BOX / 2 TABLET in 1 POUCH
Product Code
68737-232
11-Digit Billing Format
68737023216
RxNorm Crosswalk
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet

Clinical Specifications

Proprietary Name
Conrx Cold
Dosage Form
-
Usage Information
• do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets every 4 hours swallow whole - do not crush, chew or dissolvedo not take more than 12 caplets in 24 hourschildren under 12 yearsdo 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
Eagle Distributors,inc.
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-15-2013
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 68737-232-16 identifies a specific commercial package of 50 pouch in 1 box / 2 tablet in 1 pouch of Conrx Cold, labeled by Eagle Distributors,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 Eagle Distributors,inc. on February 15, 2013. The current certification is valid through December 31, 2017.

How is this Eagle Distributors,inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68737023216. 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)
68737-232-16
11-Digit CMS (5-4-2)
68737-0232-16

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