Thicker Fuller Hair - Dandruff Sulfate Free
NDC Package 31774-1018-1

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Thicker Fuller Hair - Dandruff Sulfate Free is wet hair, lather and rinse thoroughly. Marketed by Golden Sun Dba Newhall Laboratories, this product is identified by NDC 31774-1018 and is authorized under FDA application part358F.

Identification & Billing

NDC Package Code
31774-1018-1
Package Description
355 mL in 1 BOTTLE
Product Code
31774-1018
11-Digit Billing Format
31774101801
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Thicker Fuller Hair - Dandruff Sulfate Free
Dosage Form
-
Usage Information
Wet hair, lather and rinse thoroughly. For best results, use at least twice a week or as directed by a doctor.

Regulatory & Marketing

Labeler Name
Golden Sun Dba Newhall Laboratories
FDA Application #
part358F
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-16-2013
Listing Expiration
12-31-2017
Exclude Flag
I
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 31774-1018-1 identifies a specific commercial package of 355 ml in 1 bottle of Thicker Fuller Hair - Dandruff Sulfate Free, labeled by Golden Sun Dba Newhall Laboratories. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Golden Sun Dba Newhall Laboratories on December 16, 2013. The current certification is valid through December 31, 2017.

How is this Golden Sun Dba Newhall Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 31774101801. 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 (5-4-1)
31774-1018-1
11-Digit CMS (5-4-2)
31774-1018-01

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