Hand Sanitizer Agavespa Skincare
NDC Package 77415-000-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Hand Sanitizer Agavespa Skincare is apply enough gel to wet hands and rub together until dry.  Use 1 to 3 times daily. Marketed by Ddi Multinacional, S.a. De C.v., this product is identified by NDC 77415-000 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
77415-000-00
Package Description
1000 mL in 1 BOTTLE
Product Code
77415-000
11-Digit Billing Format
77415000000
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand Sanitizer Agavespa Skincare
Dosage Form
-
Usage Information
Apply enough gel to wet hands and rub together until dry.  Use 1 to 3 times daily.

Regulatory & Marketing

Labeler Name
Ddi Multinacional, S.a. De C.v.
FDA Application #
part333E
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
04-01-2020
End Marketing Date
07-18-2022
Listing Expiration
07-18-2022
Exclude Flag
D
Sample Package
No

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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 77415-000-00 identifies a specific commercial package of 1000 ml in 1 bottle of Hand Sanitizer Agavespa Skincare, labeled by Ddi Multinacional, S.a. De C.v.. 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 Ddi Multinacional, S.a. De C.v. on April 01, 2020. The current certification is valid through July 18, 2022.

How is this Ddi Multinacional, S.a. De C.v. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 77415000000. 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)
77415-000-00
11-Digit CMS (5-4-2)
77415-0000-00

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