Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women
NDC Package 69423-558-01

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 discontinued by the firm.

Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women is apply one mL with dropper 2 times a day directly onto the scalp in the hair loss areausing more or more often will not improve resultscontinued use is necessary to increase and keep your hair regrowth, or hair loss will begin again. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 69423-558 and is authorized under FDA application ANDA091344.

Identification & Billing

NDC Package Code
69423-558-01
Package Description
3 BOTTLE, DROPPER in 1 CARTON / 60 mL in 1 BOTTLE, DROPPER
Product Code
69423-558
11-Digit Billing Format
69423055801

Clinical Specifications

Proprietary Name
Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women
Dosage Form
-
Usage Information
Apply one mL with dropper 2 times a day directly onto the scalp in the hair loss areausing more or more often will not improve resultscontinued use is necessary to increase and keep your hair regrowth, or hair loss will begin again

Regulatory & Marketing

Labeler Name
The Procter & Gamble Manufacturing Company
FDA Application #
ANDA091344
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-15-2023
End Marketing Date
05-01-2026
Listing Expiration
05-01-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 69423-558-01 identifies a specific commercial package of 3 bottle, dropper in 1 carton / 60 ml in 1 bottle, dropper of Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women, labeled by The 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 The Procter & Gamble Manufacturing Company on January 15, 2023. The current certification is valid through May 01, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69423055801. 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)
69423-558-01
11-Digit CMS (5-4-2)
69423-0558-01

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