Ido Clean Gel Alpha Hand Sanitizer
NDC Package 77039-073-50
Package Information
Ido Clean Gel Alpha Hand Sanitizer is a . Marketed by Ido Pharm, this product is identified by NDC 77039-073 and is authorized under FDA application part333A.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 77039 - Ido Pharm
- 77039-073 - Ido Clean Gel Alpha Hand Sanitizer
- 77039-073-50 - 500 mL in 1 BOTTLE, PLASTIC
- 77039-073 - Ido Clean Gel Alpha Hand Sanitizer
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 77039-073-50 identifies a specific commercial package of 500 ml in 1 bottle, plastic of Ido Clean Gel Alpha Hand Sanitizer, labeled by Ido Pharm. 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 Ido Pharm on May 30, 2020. The current certification is valid through December 24, 2021.
How is this Ido Pharm product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 77039007350. 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.