Osong Antiseptic Alcohol
NDC Package 81294-0002-1
Package Information
Osong Antiseptic Alcohol is a . Marketed by Osong Co., Ltd., this product is identified by NDC 81294-0002 and is authorized under FDA application part333A.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 81294 - Osong Co., Ltd.
- 81294-0002 - Osong Antiseptic Alcohol
- 81294-0002-1 - 500 mL in 1 POUCH
- 81294-0002 - Osong Antiseptic 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 81294-0002-1 identifies a specific commercial package of 500 ml in 1 pouch of Osong Antiseptic Alcohol, labeled by Osong Co., Ltd.. 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 Osong Co., Ltd. on December 25, 2020. The current certification is valid through December 25, 2020.
How is this Osong Co., Ltd. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 81294000201. 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 Package segment to maintain the 5-4-2 structure.