Selenium Sulfide Slurry Pre-mix Solution
NDC Package 69423-110-01

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 an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Selenium Sulfide Slurry Pre-mix solution is a medication used to treat dandruff and a certain scalp infection (seborrheic dermatitis). This formulation utilizes a solution delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 69423-110.

Identification & Billing

NDC Package Code
69423-110-01
Package Description
100 kg in 1 DRUM
Product Code
69423-110
11-Digit Billing Format
69423011001

Clinical Specifications

Proprietary Name
Selenium Sulfide Slurry Pre-mix
Non-Proprietary Name
Selenium Sulfide Slurry Pre-mix
Substance Name
Selenium Sulfide
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Active Ingredient(s)
SELENIUM SULFIDE 29.41 kg/100kg
Usage Information
This medication is used to treat dandruff and a certain scalp infection (seborrheic dermatitis). It reduces itching, flaking, irritation, and redness of the scalp. Selenium sulfide is also used for a condition that causes discoloration of the skin (tinea versicolor). This medication belongs to a class of medications called anti-infectives. It works by slowing the growth of the yeast that causes the infection.

Regulatory & Marketing

Labeler Name
The Procter & Gamble Manufacturing Company
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
08-19-2010
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 69423-110-01 identifies a specific commercial package of 100 kg in 1 drum of Selenium Sulfide Slurry Pre-mix (UNFINISHED drug), drug for further processing labeled by The Procter & Gamble Manufacturing Company. This solution is formulated for use and contains selenium sulfide 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 The Procter & Gamble Manufacturing Company on August 19, 2010. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

This medication is used to treat dandruff and a certain scalp infection (seborrheic dermatitis). It reduces itching, flaking, irritation, and redness of the scalp. Selenium sulfide is also used for a condition that causes discoloration of the skin (tinea versicolor). This medication belongs to a class of medications called anti-infectives. It works by slowing the growth of the yeast that causes the infection.

How is this The Procter & Gamble Manufacturing Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69423011001. 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)
69423-110-01
11-Digit CMS (5-4-2)
69423-0110-01

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