GUNA STOMACH PLUS

ANTIMONIUM CRUDUM - ARGENTUM NITRICUM - ARSENICUM ALBUM - IPECACUANHA - NUX VOMICA - ORIGANUM MAJORANA - CUPRUM METALLICUM - TARAXACUM OFFICINALE - NATRUM PHOSPHORICUM - ORAL HUMAN OTC DRUG

GUNA STOMACH PLUS is an FDA drug label for the active ingredient ANTIMONIUM CRUDUM - ARGENTUM NITRICUM - ARSENICUM ALBUM - IPECACUANHA - NUX VOMICA - ORIGANUM MAJORANA - CUPRUM METALLICUM - TARAXACUM OFFICINALE - NATRUM PHOSPHORICUM - 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 20211215.

Generic name
ANTIMONIUM CRUDUM - ARGENTUM NITRICUM - ARSENICUM ALBUM - IPECACUANHA - NUX VOMICA - ORIGANUM MAJORANA - CUPRUM METALLICUM - TARAXACUM OFFICINALE - NATRUM PHOSPHORICUM -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-477
Application
N/A
Label effective
20211215

About this product

GUNA STOMACH PLUS is an FDA-registered drug product whose active ingredient is ANTIMONIUM CRUDUM - ARGENTUM NITRICUM - ARSENICUM ALBUM - IPECACUANHA - NUX VOMICA - ORIGANUM MAJORANA - CUPRUM METALLICUM - TARAXACUM OFFICINALE - NATRUM PHOSPHORICUM -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-477, label effective 20211215. 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 ANTIMONIUM CRUDUM - ARGENTUM NITRICUM - ARSENICUM ALBUM - IPECACUANHA - NUX VOMICA - ORIGANUM MAJORANA - CUPRUM METALLICUM - TARAXACUM OFFICINALE - NATRUM PHOSPHORICUM - are most often described in connection with: relieves symptoms, acid reflux, heartburn sour, stomach nausea. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS/PURPOSE Antimonium crudum 6X Relieves heartburn Argentum nitricum 6X Relieves heartburn Arsenicum album 6X Relieves indigestion and nausea Ipecacuanha 8X, 30X, 200X Relieves nausea and vomiting Nux vomica 4X Relieves heartburn, stomach pain Origanum majorana 6X Loss of appetite, hiccough Cuprum metallicum 4X Relieves stomach cramps Taraxacum officinale 6X Relieves heartburn, sour stomach Natrum phosphoricum 4X Relieves heartburn, sour stomach

Indications & Usage

Relieves symptoms of acid reflux and gastritis such as: heartburn sour stomach nausea after eating

Dosage & Administration

Adults and children 12 years and older 5 pellets 3 times per day Children between 12 and 6 years of age 3 pellets 3 times per day Children under 6 years 1 pellet 3 times per day to be disoolved 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 STOMACH PLUS used for?
Relieves symptoms of acid reflux and gastritis such as: heartburn sour stomach nausea after eating

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

What form does GUNA STOMACH 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 STOMACH 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 STOMACH 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.