NDC 17089-460 Guna Matrix Detox

Sodium Sulfate - Podophyllum Peltatum Root - Solidago Virgaurea Flowering Top - Apis Mellifera - Equisetum Hyemale - Strychnos Nux Vomica Seed - Hamamelis Virginiana Root Bark Stem Bark - Lycopodium Clavatum Spore - Galium Aparine Whole - Thuja Occidentalis Leafy Twig - Berberis Vulgaris Root Bark - Myosotis Arvensis - Chelidonium Majus Whole - Fucus Vesiculosus -

NDC Product Code 17089-460

NDC CODE: 17089-460

Proprietary Name: Guna Matrix Detox What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Sodium Sulfate - Podophyllum Peltatum Root - Solidago Virgaurea Flowering Top - Apis Mellifera - Equisetum Hyemale - Strychnos Nux Vomica Seed - Hamamelis Virginiana Root Bark Stem Bark - Lycopodium Clavatum Spore - Galium Aparine Whole - Thuja Occidentalis Leafy Twig - Berberis Vulgaris Root Bark - Myosotis Arvensis - Chelidonium Majus Whole - Fucus Vesiculosus - What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 17089 - Guna Spa

NDC 17089-460-18

Package Description: 1 BOTTLE, DROPPER in 1 BOX > 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Guna Matrix Detox with NDC 17089-460 is a a human over the counter drug product labeled by Guna Spa. The generic name of Guna Matrix Detox is sodium sulfate - podophyllum peltatum root - solidago virgaurea flowering top - apis mellifera - equisetum hyemale - strychnos nux vomica seed - hamamelis virginiana root bark stem bark - lycopodium clavatum spore - galium aparine whole - thuja occidentalis leafy twig - berberis vulgaris root bark - myosotis arvensis - chelidonium majus whole - fucus vesiculosus -. The product's dosage form is solution/ drops and is administered via oral form.

Labeler Name: Guna Spa

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Guna Matrix Detox Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SODIUM SULFATE 12 [hp_X]/30mL
  • SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 2 [hp_X]/30mL
  • URTICA URENS WHOLE 6 [hp_X]/30mL
  • RANCID BEEF 12 [hp_X]/30mL
  • SODIUM PYRUVATE 3 [hp_X]/30mL
  • FUCUS VESICULOSUS 6 [hp_X]/30mL
  • SUS SCROFA VEIN 6 [hp_X]/30mL
  • GALIUM APARINE WHOLE 4 [hp_X]/30mL
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/30mL
  • CONIUM MACULATUM FLOWERING TOP 3 [hp_X]/30mL
  • MYOSOTIS ARVENSIS 4 [hp_X]/30mL
  • MALIC ACID 6 [hp_X]/30mL
  • GRAPHITE 12 [hp_X]/30mL
  • SILICON DIOXIDE 8 [hp_X]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Guna Spa
Labeler Code: 17089
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 07-14-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Guna Matrix Detox Product Label Images

Guna Matrix Detox Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient(S)

Active ingredient PurposeMalicum Acidum 6X detoxificationFucus vesiculosus 6X detoxificationThuja occidentalis 6X detoxification drainageUrtica urens 6X detoxificationNatrum sulphuricum 12X detoxificationPyrogenium 12X detoxificationNatrum oxalaceticum 3X Relieves skin rashesNatrum pyruvicum 3X Relieves skin rashesGraphites 12X Relieves skin rashesMyosotis arvensis 4X Helps venous and lymphatic flowVena suis 6X Helps venous and lymphatic flowSolidago virgaurea 2X Helps kidney functionConium maculatum 3X Relieves fatigueGalium aparine 4X Increases urinationSilicea 8X Relieves fatigue

Purpose

  • HELPS ELIMINATE TOXINS, RELIEVES SYMPTOMS OF TOXIN BUILDUP, SUCH AS:FatigueSkin rashesSwelling

Indications & Usage

Take 15 minutes before meals

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 accidental overdose, seek prfessional assistance or contact a Poison Control Center immediatelyContains ethyl alcohol 30%

Do Not Use

If tamper-evident seal is broken

Otc - When Using

Helps eliminate toxins, relieves symptoms of toxin buildup, such as:
fatigue, skin rashes, swelling.

Otc - Stop Use

Stop use and ask doctor if symptoms persist more than 5 days.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

Take 15 minutes before meals.Adults and children twelve years and older: 20 drops in a little water, 2 times per dayChildren between 12 years and 6 years of age: 10 drops in a little water, 2 times per dayChildren under 6 years: consult a physician

Other Information

  • No special storage conditions

Inactive Ingredients

Inactive Ingredient: Ethyl alcohol 30%

Recent Major Changes

Not applicable

Adverse Reactions

To Report SUSPECTED ADVERSE REACTIONS, contact Guna Inc at (484) 223-3500 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

* Please review the disclaimer below.