GUNA DEFENSE

CALCIUM SULFIDE - CENTELLA ASIATICA - ECHINACEA ANGUSTIFOLIA WHOLE - ECHINACEA PURPUREA - THUJA OCCIDENTALIS LEAFY TWIG - VINCETOXICUM HIRUNDINARIA ROOT - PHYTOLACCA AMERICANA ROOT - SULFUR - ORAL HUMAN OTC DRUG

GUNA DEFENSE is an FDA drug label for the active ingredient CALCIUM SULFIDE - CENTELLA ASIATICA - ECHINACEA ANGUSTIFOLIA WHOLE - ECHINACEA PURPUREA - THUJA OCCIDENTALIS LEAFY TWIG - VINCETOXICUM HIRUNDINARIA ROOT - PHYTOLACCA AMERICANA ROOT - SULFUR - 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
CALCIUM SULFIDE - CENTELLA ASIATICA - ECHINACEA ANGUSTIFOLIA WHOLE - ECHINACEA PURPUREA - THUJA OCCIDENTALIS LEAFY TWIG - VINCETOXICUM HIRUNDINARIA ROOT - PHYTOLACCA AMERICANA ROOT - SULFUR -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-467
Application
N/A
Label effective
20211215

About this product

GUNA DEFENSE is an FDA-registered drug product whose active ingredient is CALCIUM SULFIDE - CENTELLA ASIATICA - ECHINACEA ANGUSTIFOLIA WHOLE - ECHINACEA PURPUREA - THUJA OCCIDENTALIS LEAFY TWIG - VINCETOXICUM HIRUNDINARIA ROOT - PHYTOLACCA AMERICANA ROOT - SULFUR -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-467, 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 CALCIUM SULFIDE - CENTELLA ASIATICA - ECHINACEA ANGUSTIFOLIA WHOLE - ECHINACEA PURPUREA - THUJA OCCIDENTALIS LEAFY TWIG - VINCETOXICUM HIRUNDINARIA ROOT - PHYTOLACCA AMERICANA ROOT - SULFUR - are most often described in connection with: relieves respiratory, intestinal symptoms, viral infections, cough sore, throat cold, sores fever. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS/PURPOSE Asclepias vincetoxicum 6X Relieves fever of viral origin Echinacea 2X Relieves cold symptoms Echinacea purpurea 2X Relieves cold symptoms Hepar sulphuris calc. 10X Relieves painful, dry cough Hydrocotyle asiatica 4X Relieves sore throat Phytolacca decandra 4X Relieves sore throat Sulphur 10X Relieves diarrhea Thuja occidentalis 6X Relieves cold sores

Indications & Usage

Uses: Relieves respiratory or intestinal symptoms of viral infections, such as: cough, sore throat; cold sores; fever; diarrhea

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 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 DEFENSE used for?
Uses: Relieves respiratory or intestinal symptoms of viral infections, such as: cough, sore throat; cold sores; fever; diarrhea

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

What form does GUNA DEFENSE 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 DEFENSE 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 DEFENSE 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.