Mens Rogaine
NDC Package 42002-101-06

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Mens Rogaine is a . Marketed by Johnson & Johnson Consumer Inc., this product is identified by NDC 42002-101 and is authorized under FDA application NDA020834.

Identification & Billing

NDC Package Code
42002-101-06
Package Description
3 BOTTLE, PLASTIC in 1 CARTON / 60 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
42002010106

Clinical Specifications

Proprietary Name
Mens Rogaine Extra Strength
Dosage Form
-

Regulatory & Marketing

Labeler Name
Johnson & Johnson Consumer Inc.
FDA Application #
NDA020834
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
07-16-2010
End Marketing Date
12-01-2018
Listing Expiration
12-01-2018
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 (42002-101). Click a package code to view its specific billing and regulatory data.

1 BOTTLE, PLASTIC in 1 CARTON / 60 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 42002-101-06 identifies a specific commercial package of 3 bottle, plastic in 1 carton / 60 ml in 1 bottle, plastic of Mens Rogaine Extra Strength, labeled by Johnson & Johnson Consumer 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 Johnson & Johnson Consumer Inc. on July 16, 2010. The current certification is valid through December 01, 2018.

How is this Johnson & Johnson Consumer Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 42002010106. 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)
42002-101-06
11-Digit CMS (5-4-2)
42002-0101-06

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