NDC 17089-311 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 -

NDC Product Code 17089-311

NDC Code: 17089-311

Proprietary Name: Guna-liver What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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 - What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.


Code Structure
  • 17089 - Guna Spa
    • 17089-311 - Guna-liver

NDC 17089-311-20

Package Description: 2 TUBE in 1 BOX > 4 g in 1 TUBE

NDC Product Information

Guna-liver with NDC 17089-311 is a a human over the counter drug product labeled by Guna Spa. The generic name of Guna-liver is 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 -. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Guna Spa

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Guna-liver Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SILYBUM MARIANUM SEED 2 [hp_X]/4g
  • CEANOTHUS AMERICANUS LEAF 6 [hp_X]/4g
  • CHELIDONIUM MAJUS 2 [hp_X]/4g
  • CHIONANTHUS VIRGINICUS BARK 6 [hp_X]/4g
  • CHOLINE HYDROXIDE 4 [hp_X]/4g
  • COBALAMIN 4 [hp_X]/4g
  • FUMARIC ACID 4 [hp_X]/4g
  • SUS SCROFA GALLBLADDER 8 [hp_X]/4g
  • PORK LIVER 6 [hp_X]/4g
  • INOSITOL 4 [hp_X]/4g
  • SUS SCROFA JEJUNUM 8 [hp_X]/4g
  • POTASSIUM SULFATE 12 [hp_X]/4g
  • CULVER'S ROOT 6 [hp_X]/4g
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/4g
  • SODIUM DIETHYL OXALACETATE 4 [hp_X]/4g
  • SODIUM PYRUVATE 4 [hp_X]/4g
  • SODIUM SULFATE 8 [hp_X]/4g
  • NIACIN 6 [hp_X]/4g
  • SUS SCROFA PANCREAS 8 [hp_X]/4g
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/4g
  • RIBOFLAVIN 6 [hp_X]/4g
  • SUS SCROFA SPLEEN 8 [hp_X]/4g
  • TARAXACUM OFFICINALE 2 [hp_X]/4g
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/4g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • SUCROSE (UNII: C151H8M554)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Guna-liver Product Label Images

Guna-liver Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Carduus marianus    2X    DETOXIFICATIONCeanothus americanus    6X    DETOXIFICATIONChelidonium majus     2X    DETOXIFICATIONChionanthus virginica     6X    Pain relieverCholinum      4X    Stimulates digestionCobalamin     4X    ANTIOXIDANTFumaricum acidum    4X    ANTIOXIDANTGall bladder    8X    Stimulates digestionHepar    6X    Stimulates digestionInositol     4X    Stimulates digestionJejunum     8X    Stimulates digestionKali sulphuricum     6X 8x 12x    Stomach activityLeptandra virginica     6X    Stimulates digestionLycopodium clavatum     6X    LaxativeNatrum oxalaceticum    4X    ANTIOXIDANTNatrum pyruvicum     4X    ANTIOXIDANTNatrum sulphuricum    6X 8x 12x    Stomach activityNiacin     6X    Metabolic SupportPancreas    8X    Stimulates digestionPyridoxinum hydrochloricum      6X    ANTIOXIDANTRiboflavinum      6X    ANTIOXIDANTSpleen    8X    DETOXIFICATIONTaraxacum officinale     2X    LaxativeThiaminum hydrochloricum     6X    ANTIOXIDANT

Otc - Purpose

For the temporary relief of symptoms of colic and gas pains such as: bloating, general aches and pains

Otc - Stop Use

Stop use and ask doctor if symptoms of bloating, aches and pains persist more than 3 days, or if fever develops

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep this and all medicines out of reach of children

Otc - When Using

Take 15 minutes before mealsAdults and children 12 years and older    5 pellets 3 times per dayChildren between 12 years and 6 years of age   3 pellets 3 times per dayChildren under 6 years     1 pellet 3 times per day to be dissolved into a little water

Otc - Questions

Questions?: info@gunainc.comtel. (484) 223-3500

* Please review the disclaimer below.

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