Bengama Antifungal
NDC Package 69666-831-04

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.

Bengama Antifungal is shake well before usingapply generously to affected areas and massage gently until liquid is absorbed into the skinfor adults and children over 12, rub well on the afffected area. Marketed by Genuine Drugs, this product is identified by NDC 69666-831 and is authorized under FDA application part333C.

Identification & Billing

NDC Package Code
69666-831-04
Package Description
1 BOTTLE in 1 BOX / 118 mL in 1 BOTTLE
Product Code
69666-831
11-Digit Billing Format
69666083104
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Bengama Antifungal
Dosage Form
-
Usage Information
Shake well before usingapply generously to affected areas and massage gently until liquid is absorbed into the skinfor adults and children over 12, rub well on the afffected area. repeat 3-4 times dailyfor children 12 years of age or younger, consult a doctor before use

Regulatory & Marketing

Labeler Name
Genuine Drugs
FDA Application #
part333C
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-20-2015
Listing Expiration
12-31-2024
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 69666-831-04 identifies a specific commercial package of 1 bottle in 1 box / 118 ml in 1 bottle of Bengama Antifungal, labeled by Genuine Drugs. 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 Genuine Drugs on April 20, 2015. The current certification is valid through December 31, 2024.

How is this Genuine Drugs product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69666083104. 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)
69666-831-04
11-Digit CMS (5-4-2)
69666-0831-04

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