GUNA-RHINO NOSE

APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE - ORAL HUMAN OTC DRUG

GUNA-RHINO NOSE is an FDA drug label for the active ingredient APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE - 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
APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-419
Application
N/A
Label effective
20181221

About this product

GUNA-RHINO NOSE is an FDA-registered drug product whose active ingredient is APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-419, 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 APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE - are most often described in connection with: tilt head, slightly forward, place tip, nose compress, spray aiming. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS/PURPOSE ALIUM CEPA 6X, 8X, 12X EXPECTORANT APIS MELLIFICA 12x, 30X, 200X DECONGESTANT ARALIA RACEMOSA 1X ANTITUSSIVE ARGENTUM NITRICUM 10X ANALGESIC ASCORBIC ACID 2X ANTIOXIDANT BLACK CURRANT, BARK 1X DETOXIFICATION CISTUS CANADENSIS 4X HELPS BRONCHIAL SECRETION CUPRUM METALLICUM 4X ANTIOXIDANT EUPHORBIUM OFFICINARUM 4X MUCOLYTIC HISTAMINUM HYDROCHLORICUM 30X, 200X ANTI-INFLAMMATORY INTERFERON GAMMA 4C ANTIVIRAL INTERLEUKIN 10 4C ANTI-INFLAMMATORY INTERLEUKIN 12 4C SUPPORTS IMMUNE ACTIVITY MANGANESE GLUCONATE 4X DECONGESTANT MELILOTUS OFFICINALIS 3X DECONGESTANT PLANTAGO MAJOR 2X DETOXIFICATION ROSA CANINA, BARK 1X PAIN RELIEF SAMBUCUS NIGRA 2X ANTITUSSIVE

Indications & Usage

Tilt head slightly forward, place tip of bottle into nose, compress bottle once for each spray, aiming towards the back of the nose.

Dosage & Administration

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

Warnings

WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 5 days

Frequently asked questions

What is GUNA-RHINO NOSE used for?
Tilt head slightly forward, place tip of bottle into nose, compress bottle once for each spray, aiming towards the back of the nose.

Who makes GUNA-RHINO NOSE?
Guna spa is the labeler of record for GUNA-RHINO NOSE.

What form does GUNA-RHINO NOSE 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-RHINO NOSE 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-RHINO NOSE 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.