GUNA-REACT

ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC - ORAL HUMAN OTC DRUG

GUNA-REACT is an FDA drug label for the active ingredient ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC - 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
ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
17089-237
Application
N/A
Label effective
20181221

About this product

GUNA-REACT is an FDA-registered drug product whose active ingredient is ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-237, 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 ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC - are most often described in connection with: directions turn, tube upside, rotate cap, release pellets, without touching, tip them, tongue allow, dissolve take. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS/PURPOSE ANGELICA SINENSIS, RADIX 3X DETOXIFICATION ARNICA MONTANA 4X, 6X, 8X ANTI-INFLAMMATION CARDUUS MARIANUS 3X DETOXIFICATION ECHINACEA ANGUSTIFOLIA 3X IMMUNE SUPPORT GINSENG 1X IMPROVE STAMINA HEPAR 4C DETOXIFICATION INTERFERON GAMMA 4C 7C IMMUNE SUPPORT LING CHI MUSHROOM 8X ANTIOXIDANT LYMPHATIC GLAND 4C IMMUNE SUPPORT PAEONIA OFFICINALIS 3X IMMUNE SUPPORT TURKEY TAIL 8X ANTIOXIDANT TURMERIC 3X PAIN RELIEF

Indications & Usage

Directions : Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.

Dosage & Administration

DIRECTIONS Take 15 minutes before meals Adults and children 12 years and older 5 pellets 3 times per day Children between 12 years and 6 years of age 3 pellets 3 times per day Children under 6 years 1 pellet 3 times per day to be dissolved into a little water

Warnings

WARNINGS Stop use and ask doctor if symptoms of discomfort with swallowing or run down feeling worsen or persist more than 5 days

Frequently asked questions

What is GUNA-REACT used for?
Directions : Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.

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

What form does GUNA-REACT 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-REACT 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-REACT 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.