GUNA THROAT AND GUMS

ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL - ORAL HUMAN OTC DRUG

GUNA THROAT AND GUMS is an FDA drug label for the active ingredient ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL - 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 20210217.

Generic name
ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-479
Application
N/A
Label effective
20210217

About this product

GUNA THROAT AND GUMS is an FDA-registered drug product whose active ingredient is ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-479, label effective 20210217. 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 ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL - are most often described in connection with: directions rotate, upright position, spray needed, onto affected, areas mouth, throat gums. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS/PURPOSE Aconitum napellus 3X Arnica montana 3X Belladonna 4X Echinacea 2X Echinacea purpurea 2X Hamamelis virginiana 2X Hepar sulphuris calcareum 6X Hypericum perforatum 3X Millefolium 3X Symphytum officinale 6X RELIEF OF INFLAMMATION AND PAIN

Indications & Usage

Directions : Rotate the sprayer to the upright position. Spray as needed onto affected areas: mouth, throat, or gums.

Dosage & Administration

DIRECTIONS Adults and children 12 years and older 2 sprays, 3-5 times per day Children between 12 and 6 years of age 1 spray, 3-5 times per day Children under 6 years consult a physician

Warnings

WARNINGS Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a health professional promptly. ●Stop use and ask doctor if symptoms persist more than 3 days. ● If pregnant or breast-feeding ask a health care professional before use.● Keep out of reach of children. In case of overdose, get medical seek professional assistance or contact a Poison Control Center immediately. ● Contains ethyl alcohol 20%

Frequently asked questions

What is GUNA THROAT AND GUMS used for?
Directions : Rotate the sprayer to the upright position. Spray as needed onto affected areas: mouth, throat, or gums.

Who makes GUNA THROAT AND GUMS?
Guna spa is the labeler of record for GUNA THROAT AND GUMS.

What form does GUNA THROAT AND GUMS 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 THROAT AND GUMS 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 THROAT AND GUMS 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.