Solenal Sulv Disinfectant
NDC Package 76761-101-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Solenal Sulv Disinfectant is direct wipe or press spray to achieve germicidal efficacy. Marketed by Shui Yi Ren Technology Development Co., Ltd., this product is identified by NDC 76761-101.

Identification & Billing

NDC Package Code
76761-101-01
Package Description
50 mL in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
76761010101

Clinical Specifications

Proprietary Name
Solenal Sulv Disinfectant
Dosage Form
-
Usage Information
Direct wipe or press spray to achieve germicidal efficacy.

Regulatory & Marketing

Labeler Name
Shui Yi Ren Technology Development Co., Ltd.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
05-22-2020
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
Yes

Hierarchy Structure

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (76761-101). Click a package code to view its specific billing and regulatory data.

100 mL in 1 BOTTLE, SPRAY

* 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 76761-101-01 identifies a specific commercial package of 50 ml in 1 bottle, spray of Solenal Sulv Disinfectant, labeled by Shui Yi Ren Technology Development 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 Shui Yi Ren Technology Development Co., Ltd. on May 22, 2020. The current certification is valid through December 31, 2021.

How is this Shui Yi Ren Technology Development Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76761010101. 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)
76761-101-01
11-Digit CMS (5-4-2)
76761-0101-01

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