Guna-liver Pellet
NDC Package 17089-311-20

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

Package Information

Guna-liver (ceanothus americanus leaf - chelidonium majus - chionanthus virginicus bark - choline hydroxide - cobalamin - culver root - fumaric acid - inositol - lycopodium clavatum spore - niacin - pork liver - potassium sulfate - pyridoxine hydrochloride - riboflavin - silybum marianum seed - sodium diethyl oxalacetate - sodium pyruvate - sodium sulfate - sus scrofa gall bladder - sus scrofa jejunum - sus scrofa pancreas - sus scrofa spleen - taraxacum officinale - thiamine hydrochloride -) pellets is a medication used as For the temporary relief of symptoms of colic and gas pains such as: bloating, general aches and pains. This formulation utilizes a pellet delivery system. Marketed by Guna Spa, this product is identified by NDC 17089-311.

Identification & Billing

NDC Package Code
17089-311-20
Package Description
2 TUBE in 1 BOX / 4 g in 1 TUBE
Product Code
17089-311
11-Digit Billing Format
17089031120

Clinical Specifications

Proprietary Name
Guna-liver
Non-Proprietary Name
Ceanothus Americanus Leaf - Chelidonium Majus - Chionanthus Virginicus Bark - Choline Hydroxide - Cobalamin - Culver Root - Fumaric Acid - Inositol - Lycopodium Clavatum Spore - Niacin - Pork Liver - Potassium Sulfate - Pyridoxine Hydrochloride - Riboflavin - Silybum Marianum Seed - Sodium Diethyl Oxalacetate - Sodium Pyruvate - Sodium Sulfate - Sus Scrofa Gall Bladder - Sus Scrofa Jejunum - Sus Scrofa Pancreas - Sus Scrofa Spleen - Taraxacum Officinale - Thiamine Hydrochloride -
Substance Name
Ceanothus Americanus Leaf; Chelidonium Majus; Chionanthus Virginicus Bark; Choline Hydroxide; Cobalamin; Culver's Root; Fumaric Acid; Inositol; Lycopodium Clavatum Spore; Niacin; Pork Liver; Potassium Sulfate; Pyridoxine Hydrochloride; Riboflavin; Silybum Marianum Seed; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Sodium Sulfate; Sus Scrofa Gallbladder; Sus Scrofa Jejunum; Sus Scrofa Pancreas; Sus Scrofa Spleen; Taraxacum Officinale; Thiamine Hydrochloride
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
This product is used as For the temporary relief of symptoms of colic and gas pains such as: bloating, general aches and pains

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
05-23-2006
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 17089-311-20 identifies a specific commercial package of 2 tube in 1 box / 4 g in 1 tube of Guna-liver, a human over the counter drug labeled by Guna Spa. This pellet is formulated for oral use and contains ceanothus americanus leaf; chelidonium majus; chionanthus virginicus bark; choline hydroxide; cobalamin; culver's root; fumaric acid; inositol; lycopodium clavatum spore; niacin; pork liver; potassium sulfate; pyridoxine hydrochloride; riboflavin; silybum marianum seed; sodium diethyl oxalacetate; sodium pyruvate; sodium sulfate; sus scrofa gallbladder; sus scrofa jejunum; sus scrofa pancreas; sus scrofa spleen; taraxacum officinale; thiamine hydrochloride 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 May 23, 2006. 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: 17089031120. 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)
17089-311-20
11-Digit CMS (5-4-2)
17089-0311-20

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