GUNA-MATRIX

ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - PHENYLALANINE - PRASTERONE - PROLACTIN - RANCID BEEF - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA CONJUNCTIVA - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - THUJA OCCIDENTALIS TWIG - TYROSINE - ORAL HUMAN OTC DRUG

GUNA-MATRIX is an FDA drug label for the active ingredient ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - PHENYLALANINE - PRASTERONE - PROLACTIN - RANCID BEEF - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA CONJUNCTIVA - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - THUJA OCCIDENTALIS TWIG - TYROSINE - 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 20260611.

Generic name
ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - PHENYLALANINE - PRASTERONE - PROLACTIN - RANCID BEEF - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA CONJUNCTIVA - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - THUJA OCCIDENTALIS TWIG - TYROSINE -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-416
Application
N/A
Label effective
20260611

About this product

GUNA-MATRIX is an FDA-registered drug product whose active ingredient is ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - PHENYLALANINE - PRASTERONE - PROLACTIN - RANCID BEEF - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA CONJUNCTIVA - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - THUJA OCCIDENTALIS TWIG - TYROSINE -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-416, label effective 20260611. 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 ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - PHENYLALANINE - PRASTERONE - PROLACTIN - RANCID BEEF - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA CONJUNCTIVA - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - THUJA OCCIDENTALIS TWIG - TYROSINE - 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 ASCORBIC ACID 4X ANTIOXIDANT CONJUNCTIVA TISSUE 6X DETOXIFICATION DEHYDROEPIANDROSTERON 6X HORMONAL SUPPORT DL-MALIC ACID 6X PROMOTE CELL METABOLISM FUCUS VESICULOSUS 4X DETOXIFICATION HISTIDINE 4X ANTI-INFLAMMATORY HYALURONIDASE 6X ANTI-INFLAMMATORY INTERLEUKIN 6 4C IMMUNE SUPPORT LACTICUM ACIDUM 4X ANTIOXIDANT LYMPHATIC VESSEL 6X IMMUNE SUPPORT NADIDUM 6X METABOLIC SUPPORT NATRUM OXALACETICUM 6X ANTIOXIDANT NATRUM PYRUVICUM 6X ANTIOXIDANT SODIUM SULFATE 6X, 8X, 12X, 30X, 200X ANTIOXIDANT PHENYLALANINE 4X IMPROVE CONCENTRATION PROLACTIN 6X IMPROVE CONCENTRATION PYROGENIUM 12X ANTI-INFLAMMATORY THUJA OCCIDENTALIS 6X, 8X, 12X, 30X, 200X DETOXIFICATION TRICHINOYL PHOSPHATE 6X ANTIOXIDANT TYROSINE 4X IMMUNE SUPPORT

Indications & Usage

Take 15 minutes before meals

Dosage & Administration

DIRECTIONS 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 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-MATRIX used for?
Take 15 minutes before meals

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

What form does GUNA-MATRIX 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-MATRIX 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-MATRIX 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.