Fluendz Spray
NDC Package 50367-100-01

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 approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Fluendz (asafoetida, astragalus menziesii, illicium anisatum, lonicera zylosteum) sprays is for relief of symptoms associated with the flu and common cold as per Homeopathic Materia Medica. This formulation utilizes a spray delivery system. Marketed by Herbology International Llc, this product is identified by NDC 50367-100.

Identification & Billing

NDC Package Code
50367-100-01
Package Description
20 mL in 1 BOTTLE
Product Code
50367-100
11-Digit Billing Format
50367010001

Clinical Specifications

Proprietary Name
Fluendz
Non-Proprietary Name
Asafoetida, Astragalus Menziesii, Illicium Anisatum, Lonicera Zylosteum
Substance Name
Asafetida; Astragalus Nuttallii Leaf; Star Anise; Lonicera Xylosteum Fruit
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
For relief of symptoms associated with the flu and common cold as per Homeopathic Materia Medica.

Regulatory & Marketing

Labeler Name
Herbology International Llc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-15-2010
End Marketing Date
08-31-2026
Exclude Flag
N
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 50367-100-01 identifies a specific commercial package of 20 ml in 1 bottle of Fluendz, a human over the counter drug labeled by Herbology International Llc. This spray is formulated for oral use and contains asafetida; astragalus nuttallii leaf; star anise; lonicera xylosteum fruit as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Herbology International Llc on January 15, 2010.

How is this Herbology International Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50367010001. 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)
50367-100-01
11-Digit CMS (5-4-2)
50367-0100-01

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