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  5. NDC Package Code: 83299-023-02 5% Minoxidil Foam

NDC Package 83299-023-02 5% Minoxidil Foam

Spray, Suspension Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
83299-023-02
Package Description:
60 g in 1 BOTTLE
Product Code:
83299-023
Proprietary Name:
5% Minoxidil Foam
Non-Proprietary Name:
5% Minoxidil Foam
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:
83299002302
Product Type:
Human Otc Drug
Labeler Name:
Consilii Llc
Dosage Form:
Spray, Suspension - A liquid preparation containing solid particles dispersed in a liquid vehicle and in the form of coarse droplets or as finely divided solids to be applied locally, most usually to the nasal-pharyngeal tract, or topically to the skin.
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):
  • MINOXIDIL 5 g/100g
    • Pharmacologic Class(es):
  • Arteriolar Vasodilation - [PE] (Physiologic Effect)
  • Arteriolar Vasodilator - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-08-2023
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    83299-023-0160 g in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 83299-023-02?

    The NDC Packaged Code 83299-023-02 is assigned to a package of 60 g in 1 bottle of 5% Minoxidil Foam, a human over the counter drug labeled by Consilii Llc. The product's dosage form is spray, suspension and is administered via topical form.

    Is NDC 83299-023 included in the NDC Directory?

    Yes, 5% Minoxidil Foam with product code 83299-023 is active and included in the NDC Directory. The product was first marketed by Consilii Llc on October 08, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 83299-023-02?

    The 11-digit format is 83299002302. 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
    5-3-283299-023-025-4-283299-0023-02