Ethyl Alcohol
NDC Package 59448-009-01
Package Information
Ethyl Alcohol is a . Marketed by Asp Global, this product is identified by NDC 59448-009 and is authorized under FDA application M003.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 59448 - Asp Global
- 59448-009 - Ethyl Alcohol
- 59448-009-01 - 80 APPLICATOR in 1 PACKAGE / 5.2 mL in 1 APPLICATOR
- 59448-009 - Ethyl Alcohol
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 the distribution configuration for this product package?
The code 59448-009-01 identifies a specific commercial package of 80 applicator in 1 package / 5.2 ml in 1 applicator of Ethyl Alcohol, labeled by Asp Global. 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 Asp Global on November 18, 2021. The current certification is valid through December 01, 2025.
How is this Asp Global product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 59448000901. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.