NDC Package 69423-586-01 Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women

Minoxidil Aerosol, Foam Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69423-586-01
Package Description:
3 CAN in 1 CARTON / 60 g in 1 CAN
Product Code:
Proprietary Name:
Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women
Non-Proprietary Name:
Minoxidil
Substance Name:
Minoxidil
Usage Information:
Minoxidil is used with other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Minoxidil works by relaxing blood vessels so blood can flow more easily.
11-Digit NDC Billing Format:
69423058601
NDC to RxNorm Crosswalk:
  • RxCUI: 2584341 - Head & Shoulders Scalp X 5 % Topical Foam
  • RxCUI: 2584341 - minoxidil 50 MG/ML Topical Foam [Head & Shoulders Scalp X]
  • RxCUI: 2584341 - Head & Shoulders Scalp X 50 MG/ML Topical Foam
  • RxCUI: 645146 - minoxidil 5 % Topical Foam
  • RxCUI: 645146 - minoxidil 50 MG/ML Topical Foam
  • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA091344
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-01-2021
    End Marketing Date:
    12-15-2024
    Exclude Flag:
    N

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 69423-586-01?

    The NDC Packaged Code 69423-586-01 is assigned to a package of 3 can in 1 carton / 60 g in 1 can of Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is aerosol, foam and is administered via topical form.

    Is NDC 69423-586 included in the NDC Directory?

    Yes, Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women with product code 69423-586 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on November 01, 2021.

    What is the 11-digit format for NDC 69423-586-01?

    The 11-digit format is 69423058601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-269423-586-015-4-269423-0586-01