Ethyl Alcohol
NDC Package 74331-080-01
Package Information
Ethyl Alcohol is place enough product on hands to cover all surfaces. Marketed by Bearco, this product is identified by NDC 74331-080 and is authorized under FDA application part333A.
Identification & Billing
- RxCUI: 1039339 - ethanol 80 % Topical Solution
- RxCUI: 1039339 - ethanol 0.8 ML/ML Topical Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 74331 - Bearco
- 74331-080 - Ethyl Alcohol
- 74331-080-01 - 750 mL in 1 BOTTLE
- 74331-080 - 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 74331-080-01 identifies a specific commercial package of 750 ml in 1 bottle of Ethyl Alcohol, labeled by Bearco. 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 Bearco on June 15, 2020. The current certification is valid through December 31, 2021.
How is this Bearco product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 74331008001. 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.