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 - ORAL HUMAN OTC DRUG

GUNA-LIVER is an FDA drug label for the active ingredient 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 - manufactured by Guna spa administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20181221.

Generic 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 -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-311
Application
N/A
Label effective
20181221

About this product

GUNA-LIVER is an FDA-registered drug product whose active ingredient 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 -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-311, label effective 20181221. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing 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 - are most often described in connection with: turn tube, rotate cap, release pellets, without touching, tip them, tongue allow, dissolve take. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Carduus marianus 2X DETOXIFICATION Ceanothus americanus 6X DETOXIFICATION Chelidonium majus 2X DETOXIFICATION Chionanthus virginica 6X PAIN RELIEVER Cholinum 4X STIMULATES DIGESTION Cobalamin 4X ANTIOXIDANT Fumaricum acidum 4X ANTIOXIDANT Gall bladder 8X STIMULATES DIGESTION Hepar 6X STIMULATES DIGESTION Inositol 4X STIMULATES DIGESTION Jejunum 8X STIMULATES DIGESTION Kali sulphuricum 6X 8X 12X STOMACH ACTIVITY Leptandra virginica 6X STIMULATES DIGESTION Lycopodium clavatum 6X LAXATIVE Natrum oxalaceticum 4X ANTIOXIDANT Natrum pyruvicum 4X ANTIOXIDANT Natrum sulphuricum 6X 8X 12X STOMACH ACTIVITY Niacin 6X METABOLIC SUPPORT Pancreas 8X STIMULATES DIGESTION Pyridoxinum hydrochloricum 6X ANTIOXIDANT Riboflavinum 6X ANTIOXIDANT Spleen 8X DETOXIFICATION Taraxacum officinale 2X LAXATIVE Thiaminum hydrochloricum 6X ANTIOXIDANT

Indications & Usage

Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.

Dosage & Administration

Adults and children 12 years and older 5 pellets 3 times per day Children between 12 years and 6 years of age 3 pellets 3 times per day Children under 6 years 1 pellet 3 times per day to be dissolved into a little water

Warnings

Stop use and ask doctor if symptoms persist more than 5 days or worsen. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children.

Frequently asked questions

What is GUNA-LIVER used for?
Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.

Who makes GUNA-LIVER?
Guna spa is the labeler of record for GUNA-LIVER.

What form does GUNA-LIVER come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is GUNA-LIVER prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has GUNA-LIVER been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.