Guna Hay Fever Relief Pellet
NDC Package 17089-476-20

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

Package Information

Guna Hay Fever Relief (strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -) pellets is temporarily relieves hay fever symptoms, such as:● sneezing● coughing● inflamed, runny nose. This formulation utilizes a pellet delivery system. Marketed by Guna Spa, this product is identified by NDC 17089-476.

Identification & Billing

NDC Package Code
17089-476-20
Package Description
2 TUBE in 1 BOX / 4 g in 1 TUBE
Product Code
17089-476
11-Digit Billing Format
17089047620

Clinical Specifications

Proprietary Name
Guna Hay Fever Relief
Non-Proprietary Name
Strychnos Nux Vomica Seed - Histamine Dihydrochloride - Manganese - Schoenocaulon Officinale Seed - Apis Mellifera - Arsenic Trioxide - Silver Nitrate - Onion - Euphrasia Stricta - Galphimia Glauca Flowering Top - Sulfur -
Substance Name
Apis Mellifera; Arsenic Trioxide; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Manganese; Onion; Schoenocaulon Officinale Seed; Silver Nitrate; Strychnos Nux-vomica Seed; Sulfur
Dosage Form
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Temporarily relieves hay fever symptoms, such as:● sneezing● coughing● inflamed, runny nose

Regulatory & Marketing

Labeler Name
Guna Spa
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
02-17-2021
Listing Expiration
12-31-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (17089-476). Click a package code to view its specific billing and regulatory data.

17089-476-21
1 TUBE in 1 BOX / 4 g in 1 TUBE

* 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 17089-476-20 identifies a specific commercial package of 2 tube in 1 box / 4 g in 1 tube of Guna Hay Fever Relief, a human over the counter drug labeled by Guna Spa. This pellet is formulated for oral use and contains apis mellifera; arsenic trioxide; euphrasia stricta; galphimia glauca flowering top; histamine dihydrochloride; manganese; onion; schoenocaulon officinale seed; silver nitrate; strychnos nux-vomica seed; sulfur 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 Guna Spa on February 17, 2021. The current certification is valid through December 31, 2026.

How is this Guna Spa product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17089047620. 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)
17089-476-20
11-Digit CMS (5-4-2)
17089-0476-20

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