GUNA BOWEL PLUS

ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE - ORAL HUMAN OTC DRUG

GUNA BOWEL PLUS is an FDA drug label for the active ingredient ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE - 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 20210117.

Generic name: ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
Route: ORAL
Dosage form: N/A
NDC: 17089-470
Application: N/A
Label effective: 20210117

About this product

GUNA BOWEL PLUS is an FDA-registered drug product whose active ingredient is ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-470, label effective 20210117. 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 ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE - are most often described in connection with: take minutes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS/PURPOSE Aloe 4X Relieves constipation Alumina 6X, 8X Relieves constipation Bryonia 6X, 8X Relieves nausea, appetite disorders Carbo vegetabilis 6X Helps digestion Carduus marianus 2X Supports liver function Chelidonium majus 2X Supports liver and gallbladder function Collinsonia canadensis 2X Relieves hemorrhoids and constipation Kali carbonicum 6X, 8X, 12X Relieves abdominal gas and nausea Lycopodium clavatum 2X Supports liver function and drainage Natrum carbonicum 6X, 8X, 12X Helps digestion Nux vomica 6X, 8X Relieves abdominal gas and helps digestion Pancreas suis 6X Relieves nausea, appetite disorders Rhamnus frangula 2X Relieves nausea Rheum 2X Relieves constipation Skatolum 6X, 10X Helps digestion Taraxacum officinale 2X Supports liver and gallbladder function Thiaminum hydroc. 4X Relieves abdominal gas and helps digestion

Indications & Usage

Take 15 minutes before meals

Dosage & Administration

DIRECTIONS Adults and children 12 years and older 20 drops in a little water, 2 times per day Children between 12 years and 6 years of age 10 drops in a little water, 2 times per day Children under 6 years: consulta a physician

Warnings

WARNINGS Stop use and ask doctor if symptoms persist more than 5 days. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children . In case of accidental overdose, seek professional assitance ot or contact a Poison Control Center immediately Contains Aloe: do not use orally for more than 30 days. Contains ethyl alcohol 30%

Frequently asked questions

What is GUNA BOWEL PLUS used for?
Take 15 minutes before meals

Who makes GUNA BOWEL PLUS?
Guna spa is the labeler of record for GUNA BOWEL PLUS.

What form does GUNA BOWEL PLUS 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 BOWEL PLUS 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 BOWEL PLUS 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.