NDC 44911-0296 Metabatone

Aralia Racemosa, Avena Sativa, Berberis Vulgaris, Capsicum Annuum, Ginkgo Biloba, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Amino Acids, Bromelain, Fel Tauri, Hyaluronidase, Pancreatinum, Papain, Pepsinum, Protease, Calcarea Carbonica, Calcarea Phosphorica, Hepar Sulphuris Calcareum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, Natrum Muriaticum

NDC Product Code 44911-0296

NDC Code: 44911-0296

Proprietary Name: Metabatone 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: Aralia Racemosa, Avena Sativa, Berberis Vulgaris, Capsicum Annuum, Ginkgo Biloba, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Amino Acids, Bromelain, Fel Tauri, Hyaluronidase, Pancreatinum, Papain, Pepsinum, Protease, Calcarea Carbonica, Calcarea Phosphorica, Hepar Sulphuris Calcareum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, Natrum Muriaticum 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

  • 44911 - Energique, Inc.
    • 44911-0296 - Metabatone

NDC 44911-0296-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Metabatone with NDC 44911-0296 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Metabatone is aralia racemosa, avena sativa, berberis vulgaris, capsicum annuum, ginkgo biloba, adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, amino acids, bromelain, fel tauri, hyaluronidase, pancreatinum, papain, pepsinum, protease, calcarea carbonica, calcarea phosphorica, hepar sulphuris calcareum, iodium, lycopodium clavatum, magnesia carbonica, natrum muriaticum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, Inc.

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.

Metabatone 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.

  • ARALIA RACEMOSA ROOT 3 [hp_X]/mL
  • AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • CAPSICUM 3 [hp_X]/mL
  • GINKGO 3 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 9 [hp_X]/mL
  • OXOGLURIC ACID 9 [hp_X]/mL
  • AMINO ACIDS 9 [hp_X]/mL
  • BROMELAINS 9 [hp_X]/mL
  • BOS TAURUS BILE 9 [hp_X]/mL
  • HYALURONIDASE 9 [hp_X]/mL
  • PANCRELIPASE 9 [hp_X]/mL
  • PAPAIN 9 [hp_X]/mL
  • PEPSIN 9 [hp_X]/mL
  • BRINOLASE 9 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
  • CALCIUM SULFIDE 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • MAGNESIUM CARBONATE 12 [hp_X]/mL
  • SODIUM CHLORIDE 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)
  • 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: Energique, Inc.
Labeler Code: 44911
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: 11-17-2015 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: 01-06-2021 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.

Metabatone Product Label Images

Metabatone 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:

Aralia Racemosa 3X, Avena Sativa 3X, Berberis Vulgaris 3X, Capsicum Annuum 3X, Ginkgo Biloba 3X, Adenosinum Triphosphoricum Dinatrum 9X, 10X, 12X, Alpha-Ketoglutaricum Acidum 9X, 10X, 12X, Amino Acids 9X, 10X, 12X, Bromelain 9X, 10X, 12X, Fel Tauri 9X, 10X, 12X, Hyaluronidase 9X, 10X, 12X, Pancreatinum 9X, 10X, 12X, Papain 9X, 10X, 12X, Pepsinum 9X, 10X, 12X, Protease 9X, 10X, 12X, Calcarea Carbonica 12X, Calcarea Phosphorica 12X, Hepar Sulphuris Calcareum 12X, Iodium 12X, Lycopodium Clavatum 12X, Magnesia Carbonica 12X, Natrum Muriaticum 12X.

Indications:

For temporary relief of tiredness, weakness, general fatigue, exhaustion, weakness of memory.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For temporary relief of tiredness, weakness, general fatigue, exhaustion, weakness of memory.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breastfeeding, 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.Do not use if tamper evident seal is broken or missing.Store in a cool, dry place.

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:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 20% Ethanol.

Questions:

Dist. by Energique, Inc.201 Apple Blvd.Woodbine, IA 51579   800.868.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYMETABATONE1 fl. oz. (30 ml)

* Please review the disclaimer below.

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