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

Solution - View Billable Units, 11-Digit Format, RxNorm

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.

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:
69423-110-01
Package Description:
100 kg in 1 DRUM
Product Code:
Non-Proprietary Name:
Selenium Sulfide Slurry Pre-mix
Substance Name:
Selenium Sulfide
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.
11-Digit NDC Billing Format:
69423011001
Product Type:
Drug For Further Processing
Labeler Name:
The Procter & Gamble Manufacturing Company
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):
Sample Package:
N/A
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 Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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.

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Frequently Asked Questions

What is NDC 69423-110-01?

The NDC Packaged Code 69423-110-01 is assigned to an UNFINISHED drug package of 100 kg in 1 drum of Selenium Sulfide Slurry Pre-mix, drug for further processing labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is solution and is administered via form.

Is NDC 69423-110 included in the NDC Directory?

Yes, Selenium Sulfide Slurry Pre-mix is an UNFINISHED PRODUCT with code 69423-110 that is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on August 19, 2010 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 69423-110-01?

The 11-digit format is 69423011001. 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
5-3-269423-110-015-4-269423-0110-01