Head And Shoulders
NDC Package 37000-331-23

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.

Head And Shoulders is a . Marketed by Procter & Gamble Manufacturing Company, this product is identified by NDC 37000-331 and is authorized under FDA application part358H.

Identification & Billing

NDC Package Code
37000-331-23
Package Description
700 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
37000033123

Clinical Specifications

Proprietary Name
Head And Shoulders Itchy Scalp Care
Dosage Form
-

Regulatory & Marketing

Labeler Name
Procter & Gamble Manufacturing Company
FDA Application #
part358H
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-01-2011
End Marketing Date
11-15-2015
Listing Expiration
11-15-2015
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 (37000-331). Click a package code to view its specific billing and regulatory data.

420 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 37000-331-23 identifies a specific commercial package of 700 ml in 1 bottle, plastic of Head And Shoulders Itchy Scalp Care, 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 January 01, 2011. The current certification is valid through November 15, 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: 37000033123. 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)
37000-331-23
11-Digit CMS (5-4-2)
37000-0331-23

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