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  5. NDC Package Code: 11673-253-35 Dandruff

NDC Package 11673-253-35 Dandruff

Pyrithione Zinc 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:
11673-253-35
Package Description:
700 mL in 1 BOTTLE, PLASTIC
Product Code:
11673-253
Proprietary Name:
Dandruff
Non-Proprietary Name:
Pyrithione Zinc
Substance Name:
Pyrithione Zinc
Usage Information:
Shake wellfor maximum dandruff control, use every time you shampoowet hair, massage onto scalp, rinse, repeat if desiredfor best results use at least twice a week or as directed by a doctor
11-Digit NDC Billing Format:
11673025335
NDC to RxNorm Crosswalk:
  • RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
  • RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
  • RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Target Corporation
    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 10 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    part358H
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    12-17-2014
    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 11673-253-35?

    The NDC Packaged Code 11673-253-35 is assigned to a package of 700 ml in 1 bottle, plastic of Dandruff, a human over the counter drug labeled by Target Corporation. The product's dosage form is shampoo and is administered via topical form.

    Is NDC 11673-253 included in the NDC Directory?

    Yes, Dandruff with product code 11673-253 is active and included in the NDC Directory. The product was first marketed by Target Corporation on December 17, 2014 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 11673-253-35?

    The 11-digit format is 11673025335. 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
    5-3-211673-253-355-4-211673-0253-35