Alcohol Gel
NDC Package 52675-400-74

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. 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.

Alcohol gel is a drug for further processing. This formulation utilizes a gel delivery system. Marketed by Scribe Opco, Inc., this product is identified by NDC 52675-400.

Identification & Billing

NDC Package Code
52675-400-74
Package Description
73.9 mL in 1 BOTTLE
Product Code
52675-400
11-Digit Billing Format
52675040074

Clinical Specifications

Proprietary Name
Alcohol
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Active Ingredient(s)
ALCOHOL 62 mL/100mL

Regulatory & Marketing

Labeler Name
Scribe Opco, 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
11-05-2010
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (52675-400). Click a package code to view its specific billing and regulatory data.

52675-400-30
29.6 mL in 1 BOTTLE
52675-400-44
44 mL in 1 BOTTLE

* 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 52675-400-74 identifies a specific commercial package of 73.9 ml in 1 bottle of Alcohol (UNFINISHED drug), drug for further processing labeled by Scribe Opco, Inc.. This gel is formulated for use and contains alcohol 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 Scribe Opco, Inc. on November 05, 2010. The current certification is valid through December 31, 2026.

How is this Scribe Opco, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52675040074. 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)
52675-400-74
11-Digit CMS (5-4-2)
52675-0400-74

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