Candida Albicans, Wood Creosote, Sodium Chloride, And Sulfur Tablet
NDC Package 62982-024-01

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.

Candida Albicans, Wood Creosote, Sodium Chloride, And Sulfur tablets is a drug for further processing. This formulation utilizes a tablet delivery system. Marketed by Deseret Laboratories, Inc., this product is identified by NDC 62982-024.

Identification & Billing

NDC Package Code
62982-024-01
Package Description
33500 TABLET in 1 BOX
Product Code
62982-024
11-Digit Billing Format
62982002401

Clinical Specifications

Proprietary Name
Candida Albicans, Wood Creosote, Sodium Chloride, And Sulfur
Non-Proprietary Name
Candida Albicans, Wood Creosote, Sodium Chloride, And Sulfur
Substance Name
Candida Albicans; Sodium Chloride; Sulfur; Wood Creosote
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Deseret Laboratories, Inc.
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
04-01-2014
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 62982-024-01 identifies a specific commercial package of 33500 tablet in 1 box of Candida Albicans, Wood Creosote, Sodium Chloride, And Sulfur (UNFINISHED drug), drug for further processing labeled by Deseret Laboratories, Inc.. This tablet is formulated for use and contains candida albicans; sodium chloride; sulfur; wood creosote 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 Deseret Laboratories, Inc. on April 01, 2014. The current certification is valid through December 31, 2026.

How is this Deseret Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62982002401. 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)
62982-024-01
11-Digit CMS (5-4-2)
62982-0024-01

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