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  5. NDC Package Code: 73503-012-00 Anti Dandruff Intensive Therapy

NDC Package 73503-012-00 Anti Dandruff Intensive Therapy

Selenium Sulfide,Zinc Pyrithione,Salicylic Acid Shampoo Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
73503-012-00
Package Description:
1000 mL in 1 BOTTLE
Product Code:
73503-012
Proprietary Name:
Anti Dandruff Intensive Therapy
Non-Proprietary Name:
Selenium Sulfide, Zinc Pyrithione, Salicylic Acid
Substance Name:
Pyrithione Zinc; Salicylic Acid; Selenium Sulfide
Usage Information:
Apply shampoo to wet hair and scalp, foam, and massage onto scalp. Leave it on for 2-3 minutes. Rinse thoroughly. For best results, at least use twice a week or as directed by a doctor.
11-Digit NDC Billing Format:
73503001200
NDC to RxNorm Crosswalk:
  • RxCUI: 2672361 - salicylic acid 1 % / selenium sulfide 1 % / zinc pyrithione 1 % Medicated Shampoo
  • RxCUI: 2672361 - salicylic acid 10 MG/ML / selenium sulfide 10 MG/ML / zinc pyrithione 10 MG/ML Medicated Shampoo
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Psodex Usa Inc
    Dosage Form:
    Shampoo - A liquid soap or detergent used to clean the hair and scalp and is often used as a vehicle for dermatologic agents.
    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):
  • PYRITHIONE ZINC 1 g/100mL
  • SALICYLIC ACID 1 g/100mL
  • SELENIUM SULFIDE 1 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M032
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-01-2024
    Listing Expiration Date:
    12-31-2024
    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.

    Frequently Asked Questions

    What is NDC 73503-012-00?

    The NDC Packaged Code 73503-012-00 is assigned to a package of 1000 ml in 1 bottle of Anti Dandruff Intensive Therapy, a human over the counter drug labeled by Psodex Usa Inc. The product's dosage form is shampoo and is administered via topical form.

    Is NDC 73503-012 included in the NDC Directory?

    Yes, Anti Dandruff Intensive Therapy with product code 73503-012 is active and included in the NDC Directory. The product was first marketed by Psodex Usa Inc on January 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 73503-012-00?

    The 11-digit format is 73503001200. 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
    5-3-273503-012-005-4-273503-0012-00