GUNA-LIVER
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
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.