GUNA ALLERGY

ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA - ORAL HUMAN OTC DRUG

GUNA ALLERGY is an FDA drug label for the active ingredient ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA - 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 20201023.

Generic name: ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
Route: ORAL
Dosage form: N/A
NDC: 17089-461
Application: N/A
Label effective: 20201023

About this product

GUNA ALLERGY is an FDA-registered drug product whose active ingredient is ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-461, label effective 20201023. 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 ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA - 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 CHAMOMILLA 3X RELIEVES INFLAMMATION GLANDULA SUPRARENALIS SUIS 6X 12X 30X SUPPORTS METABOLISM MUCOSA NASALIS SUIS 200X RELIEVES ALLERGY SYMPTOMS SCILLA MARITIMA 12X 30X 200X RELIEVES DRY COUGH SABADILLA 12X 30X 200X RELIEVES HAY FEVER ALLIUM CEPA 12X 30X 200X RELIEVES RESPIRATORY CONGESTION AMMONIUM CARBONICUM 12X 30X 200X RELIEVES RESPIRATORY CONGESTION APIS MELLIFICA 200X HELPS REDUCE SWELLING ARGENTUM NITRICUM 30X RELIEVES INFLAMMATION ARSENICUM ALBUM 12X 30X 200X RELIEVES INFLAMMATION CUPRUM ACETICUM 12X 30X 200X RELIEVES HAY FEVER, PERSISTENT COUGH GALPHIMIA GLAUCA 6X 12X 200X RELIEVES HAY FEVER LUFFA OPERCULATA 6X 12X 30X RELIEVES HAY FEVER HISTAMINUM HYDROCHLORICUM 200X RELIEVES ALLERGY SYMPTOMS NATRUM MURIATICUM 12X 30X 200X RELIEVES ALLERGY SYMPTOMS ADRENALINUM 6X IMMUNE SUPPORT

Indications & Usage

Take 15 minutes before meals.

Dosage & Administration

DIRECTIONS Take 15 minutes before meals. 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: consult 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 assistance or contact a poison control center immediately. Contains ethyl alcohol 30%

Frequently asked questions

What is GUNA ALLERGY used for?
Take 15 minutes before meals.

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

What form does GUNA ALLERGY 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 ALLERGY 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 ALLERGY 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.