Doo Gro Anti-dandruff Vitalizer Cream
NDC Package 12022-005-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Doo Gro Anti-dandruff Vitalizer (pyrithione zinc) cream is apply to the affected area 1-4 times daily or as directed by a doctor. This formulation utilizes a cream delivery system. Marketed by J. Strickland & Co. Dba Nature's Protein, Inc., this product is identified by NDC 12022-005 and is authorized under FDA application M032.

Identification & Billing

NDC Package Code
12022-005-00
Package Description
100 mL in 1 JAR
Product Code
12022-005
11-Digit Billing Format
12022000500
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Doo Gro Anti-dandruff Vitalizer
Non-Proprietary Name
Pyrithione Zinc
Substance Name
Pyrithione Zinc
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
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 mg/mL
Usage Information
Apply to the affected area 1-4 times daily or as directed by a doctor.

Regulatory & Marketing

Labeler Name
J. Strickland & Co. Dba Nature's Protein, Inc.
Product Type
Human Otc Drug
FDA Application #
M032
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-15-2015
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 12022-005-00 identifies a specific commercial package of 100 ml in 1 jar of Doo Gro Anti-dandruff Vitalizer, a human over the counter drug labeled by J. Strickland & Co. Dba Nature's Protein, Inc.. This cream is formulated for topical use and contains pyrithione zinc as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by J. Strickland & Co. Dba Nature's Protein, Inc. on January 15, 2015. The current certification is valid through December 31, 2026.

How is this J. Strickland & Co. Dba Nature's Protein, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 12022000500. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
12022-005-00
11-Digit CMS (5-4-2)
12022-0005-00

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.