NDC 64578-0123 Thyropath

Avena Sativa, Borago Officinalis, Calcarea Carbonica, Chelidonium Majus, Ferrum Iodatum, Fucus Vesiculosus, Glandula Suprarenalis Suis, Hepar Suis, Iodium, Kali Iodatum, Phosphoricum Acidum, Pituitarum Posterium (bovine), Pyridoxinum Hydrochloricum, Thyroidinum (bovine), Zincum Metallicum

NDC Product Code 64578-0123

NDC Code: 64578-0123

Proprietary Name: Thyropath 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: Avena Sativa, Borago Officinalis, Calcarea Carbonica, Chelidonium Majus, Ferrum Iodatum, Fucus Vesiculosus, Glandula Suprarenalis Suis, Hepar Suis, Iodium, Kali Iodatum, Phosphoricum Acidum, Pituitarum Posterium (bovine), Pyridoxinum Hydrochloricum, Thyroidinum (bovine), Zincum Metallicum 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

  • 64578 - Energetix Corp
    • 64578-0123 - Thyropath

NDC 64578-0123-1

Package Description: 59.1 mL in 1 BOTTLE, DROPPER

NDC Product Information

Thyropath with NDC 64578-0123 is a a human over the counter drug product labeled by Energetix Corp. The generic name of Thyropath is avena sativa, borago officinalis, calcarea carbonica, chelidonium majus, ferrum iodatum, fucus vesiculosus, glandula suprarenalis suis, hepar suis, iodium, kali iodatum, phosphoricum acidum, pituitarum posterium (bovine), pyridoxinum hydrochloricum, thyroidinum (bovine), zincum metallicum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energetix Corp

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Thyropath 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.

  • AVENA SATIVA FLOWERING TOP 4 [hp_X]/mL
  • BORAGE 4 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • CHELIDONIUM MAJUS 4 [hp_X]/mL
  • FERROUS IODIDE 12 [hp_X]/mL
  • FUCUS VESICULOSUS 4 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 9 [hp_X]/mL
  • PORK LIVER 9 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • POTASSIUM IODIDE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • BOS TAURUS PITUITARY GLAND 12 [hp_X]/mL
  • PYRIDOXINE HYDROCHLORIDE 10 [hp_X]/mL
  • THYROID, BOVINE 9 [hp_X]/mL
  • ZINC 12 [hp_X]/mL

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.

  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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.

Product Labeler Information

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

Labeler Name: Energetix Corp
Labeler Code: 64578
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: 09-23-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 10-07-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Thyropath Product Label Images

Thyropath 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 Ingredients:

Avena sativa 4X, Borago officinalis 4X, Calcarea carbonica 12X, Chelidonium majus 4X, Ferrum iodatum 12X, Fucus vesiculosus 4X, Glandula suprarenalis suis 9X, 12X, 6C, Hepar suis 9X, 12X, 6C, Iodium 12X, Kali iodatum 12X, Phosphoricum acidum 12X, Pituitarum posterium (Bovine) 12X, 6C, Pyridoxinum hydrochloricum 10X, Thyroidinum (Bovine) 9X, 12X, Zincum metallicum 12X

Purpose:

Temporary relief of fatigue, cold extremities, restless sleep.

Warnings:

In case of overdose, get medical help or contact a Poison Control Center right away.If pregnant or breast feeding, ask a health professional before use.Keep out of reach of children.Other informationStore in a cool, dry place out of direct sunlight.Do not use if neck wrap is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Take 30 drops orally twice daily or as directed by a healthcare professional.Consult a physician for use in children under 12 years of age.

Uses:

Temporary relief of fatigue, cold extremities, restless sleep.

Inactive Ingredients:

Purified Water, Glycerin, 15% Ethanol.

Questions:

Distributed byEnergetix Corp.Dahlonega, GA 30533Questions?  Comments?800.990.7085www.goenergetix.com

Package Label Display:

EnergetixThyropathHomeopathic RemedyFatigue, cold extremities, restless sleep.2 fl oz (59.1 mL)

* Please review the disclaimer below.

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