GUNA-ALLERGY-PREV

AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT - ORAL HUMAN OTC DRUG

GUNA-ALLERGY-PREV is an FDA drug label for the active ingredient AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT - 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 20181221.

Generic name: AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
Route: ORAL
Dosage form: N/A
NDC: 17089-299
Application: N/A
Label effective: 20181221

About this product

GUNA-ALLERGY-PREV is an FDA-registered drug product whose active ingredient is AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-299, label effective 20181221. 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 AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT - 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 AMBROSIA ARTEMISIIFOLIA 18X RAGWEED SENSITIVITY ARUNDO MAURITANICA 18X DETOXIFICATION ACTIVITY ASCLEPIAS VINCETOXICUM 6X, 10X, 30X IMMUNE SUPPORT BLACK CURRANT 1X DETOXIFICATION ACTIVITY CITRICUM ACIDUM 6X ANTIOXIDANT HISTAMINUM HYDROCHLORICUM 12X, 30X, 200X ANTIHISTAMINE INTERFERON GAMMA 4C IMMUNE SUPPORT INTERLEUKIN 12 4C IMMUNE SUPPORT MANGANESE GLUCONATE 4X IMMUNE SUPPORT NATRUM PYRUVICUM 6X ANTI-ALLERGY NATRUM SULF 12X, 30X, 200X METABOLIC SUPPORT PARIETARIA OFFICINALIS 18X PELLITORY OF THE WALL SENSITIVITY PHLEUM PRATENSE 18X TIMOTHY SENSITIVITY SERUM ANGUILLAE 12X, 30X, 200X ANTI-ALLERGY SUCCINICUM ACIDUM 6X METABOLIC SUPPORT SULFUR 12X, 30X, 200X SKIN DETOXIFICATION URTICA URENS 18X NETTLE SENSITIVITY VIBURNUM OPULUS T LYMPHATIC SYSTEM DETOXIFICATION WYETHIA HELENIOIDES 18X WYETHIA SENSITIVITY

Indications & Usage

Take 15 minutes before meals

Dosage & Administration

DIRECTIONS For maximum symptom relief start before the anticipated allergen exposure. 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 5 drops in a glass of water, 2 times per day

Warnings

WARNINGS Stop use and ask docto r if symptoms persist more than 5 days. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Contains ethyl alcohol 30%

Frequently asked questions

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

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

What form does GUNA-ALLERGY-PREV 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-PREV 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-PREV 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.