Banda-sil Liquid Gel
NDC Package 72363-005-03

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 inactivated by the FDA.

Banda-sil Liquid Gel is indications for use:For relief of these symptoms due to minor wounds, burns, scrapes ulcerations,or minor infections, burning, stinging, itching, redness, minor pain, minor inflammation. Marketed by Ag Essence Inc, this product is identified by NDC 72363-005.

Identification & Billing

NDC Package Code
72363-005-03
Package Description
1 BOTTLE, SPRAY in 1 BOX / 28.5 g in 1 BOTTLE, SPRAY
Product Code
72363-005
11-Digit Billing Format
72363000503

Clinical Specifications

Proprietary Name
Banda-sil Liquid Gel
Dosage Form
-
Usage Information
Indications for use:For relief of these symptoms due to minor wounds, burns, scrapes ulcerations,or minor infections, burning, stinging, itching, redness, minor pain, minor inflammation.

Regulatory & Marketing

Labeler Name
Ag Essence Inc
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-25-2021
Listing Expiration
12-31-2025
Exclude Flag
I
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 72363-005-03 identifies a specific commercial package of 1 bottle, spray in 1 box / 28.5 g in 1 bottle, spray of Banda-sil Liquid Gel, labeled by Ag Essence Inc. 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 Ag Essence Inc on June 25, 2021. The current certification is valid through December 31, 2025.

How is this Ag Essence Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72363000503. 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)
72363-005-03
11-Digit CMS (5-4-2)
72363-0005-03

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