Joy
NDC Package 37000-607-12

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Joy is a . Marketed by Procter & Gamble Manufacturing Company, this product is identified by NDC 37000-607 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
37000-607-12
Package Description
375 mL in 1 BOTTLE, PLASTIC
Product Code
37000-607
11-Digit Billing Format
37000060712

Clinical Specifications

Proprietary Name
Joy Ultra Orange
Dosage Form
-

Regulatory & Marketing

Labeler Name
Procter & Gamble Manufacturing Company
FDA Application #
part333E
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
02-01-2011
End Marketing Date
10-19-2015
Listing Expiration
10-19-2015
Exclude Flag
D
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (37000-607). Click a package code to view its specific billing and regulatory data.

37000-607-25
740 mL in 1 BOTTLE, PLASTIC
37000-607-30
887 mL in 1 BOTTLE, PLASTIC

* 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 37000-607-12 identifies a specific commercial package of 375 ml in 1 bottle, plastic of Joy Ultra Orange, labeled by Procter & Gamble Manufacturing Company. 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 Procter & Gamble Manufacturing Company on February 01, 2011. The current certification is valid through October 19, 2015.

How is this Procter & Gamble Manufacturing Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37000060712. 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)
37000-607-12
11-Digit CMS (5-4-2)
37000-0607-12

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