NDC 44911-0230 Arteriotone

Baptisia Tinctoria, Cactus Grandiflorus, Echinacea (angustifolia), Adonis Vernalis, Agnus Castus, Arnica Montana, Aurum Metallicum, Digitalis Purpurea, Glonoinum, Vanadium Metallicum

  1. Labeler Index
  2. Energique, Inc.
  3. NDC: 44911-0230 Arteriotone

NDC Product Code 44911-0230

NDC CODE: 44911-0230

Proprietary Name: Arteriotone 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: Baptisia Tinctoria, Cactus Grandiflorus, Echinacea (angustifolia), Adonis Vernalis, Agnus Castus, Arnica Montana, Aurum Metallicum, Digitalis Purpurea, Glonoinum, Vanadium 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This medication is used to relieve chest pain (angina) in people that have a certain heart condition (coronary artery disease). It may also be used before physical activities (such as exercise, sexual activity) to help prevent chest pain. Nitroglycerin belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enough blood. This drug works by relaxing and widening blood vessels so blood can flow more easily to the heart.

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0230-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Arteriotone with NDC 44911-0230 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Arteriotone is baptisia tinctoria, cactus grandiflorus, echinacea (angustifolia), adonis vernalis, agnus castus, arnica montana, aurum metallicum, digitalis purpurea, glonoinum, vanadium metallicum. 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.

Arteriotone 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.
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • SELENICEREUS GRANDIFLORUS STEM 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • ADONIS VERNALIS 12 [hp_X]/mL
  • CHASTE TREE 12 [hp_X]/mL
  • ARNICA MONTANA 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • DIGITALIS 12 [hp_X]/mL
  • NITROGLYCERIN 12 [hp_X]/mL
  • VANADIUM 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.
  • 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: 07-27-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2020 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.

Arteriotone Product Label Images

Arteriotone 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:

Baptisia Tinctoria 3X, Cactus Grandiflorus 3X, Echinacea (Angustifolia) 3X, Adonis Vernalis 12X, Agnus Castus 12X, Arnica Montana 12X, Aurum Metallicum 12X, Digitalis Purpurea 12X, Glonoinum 12X, Vanadium Metallicum 12X.

Indications:

For temporary relief of swollen extremities, feel bruised, cold clammy feet, mild burning pains in lower limbs, leg cramps.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For temporary relief of swollen extremities, feel bruised, cold clammy feet, mild burning pains in lower limbs, leg cramps.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

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.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 BlvdWoodbine, IA 51579   800-869-8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYARTERIOTONE1 fl. oz. (30 ml)

* Please review the disclaimer below.