Wecare Anti-dandruff Liquid
NDC Package 67777-139-80

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

Package Information

Wecare Anti-dandruff (antidandruff shampoo) liquids is wet hairlathermassage onto scalprinse wellrepeat if desiredfor best results, use regularly. This formulation utilizes a liquid delivery system. Marketed by Dynarex Corporation, this product is identified by NDC 67777-139 and is authorized under FDA application M032.

Identification & Billing

NDC Package Code
67777-139-80
Package Description
12 BOTTLE, PLASTIC in 1 CASE / 355 mL in 1 BOTTLE, PLASTIC (67777-139-81)
Product Code
67777-139
11-Digit Billing Format
67777013980
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Wecare Anti-dandruff
Non-Proprietary Name
Antidandruff Shampoo
Substance Name
Pyrithione Zinc
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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 5 g/1000mL
Usage Information
Wet hairlathermassage onto scalprinse wellrepeat if desiredfor best results, use regularly

Regulatory & Marketing

Labeler Name
Dynarex Corporation
Product Type
Human Otc Drug
FDA Application #
M032
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-11-2018
Listing Expiration
12-31-2027
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 67777-139-80 identifies a specific commercial package of 12 bottle, plastic in 1 case / 355 ml in 1 bottle, plastic (67777-139-81) of Wecare Anti-dandruff, a human over the counter drug labeled by Dynarex Corporation. This liquid 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 Dynarex Corporation on October 11, 2018. The current certification is valid through December 31, 2027.

How is this Dynarex Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 67777013980. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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)
67777-139-80
11-Digit CMS (5-4-2)
67777-0139-80

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