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  5. NDC Package Code: 10056-006-01 Satinique Anti Dandruff

NDC Package 10056-006-01 Satinique Anti Dandruff

Pyrithione Zinc Cream 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:
10056-006-01
Package Description:
280 mL in 1 BOTTLE
Product Code:
10056-006
Proprietary Name:
Satinique Anti Dandruff
Non-Proprietary Name:
Pyrithione Zinc
Substance Name:
Pyrithione Zinc
Usage Information:
Shake well before use.Wet hair. Apply shampoo and work into a lather. Rinse thoroughly.For best result, use at least twice a week or as directed by a doctor.
11-Digit NDC Billing Format:
10056000601
NDC to RxNorm Crosswalk:
  • RxCUI: 1091088 - zinc pyrithione 0.95 % Medicated Shampoo
  • RxCUI: 1091088 - zinc pyrithione 9.5 MG/ML Medicated Shampoo
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Access Business Group Llc
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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 9.5 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M032
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-29-2017
    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 10056-006-01?

    The NDC Packaged Code 10056-006-01 is assigned to a package of 280 ml in 1 bottle of Satinique Anti Dandruff, a human over the counter drug labeled by Access Business Group Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 10056-006 included in the NDC Directory?

    Yes, Satinique Anti Dandruff with product code 10056-006 is active and included in the NDC Directory. The product was first marketed by Access Business Group Llc on March 29, 2017 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 10056-006-01?

    The 11-digit format is 10056000601. 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
    5-3-210056-006-015-4-210056-0006-01