NDC 44911-0490 Elimitone

Bellis Perennis, Echinacea (angustifolia), Trifolium Pratense, Phytolacca Decandra, Arnica Montana, Anas Barbariae, Hepatis Et Cordis Extractum, Calcarea Iodata, Kali Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Sulphur Iodatum

NDC Product Code 44911-0490

NDC Code: 44911-0490

Proprietary Name: Elimitone 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: Bellis Perennis, Echinacea (angustifolia), Trifolium Pratense, Phytolacca Decandra, Arnica Montana, Anas Barbariae, Hepatis Et Cordis Extractum, Calcarea Iodata, Kali Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Sulphur Iodatum 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.


Code Structure
  • 44911 - Energique, Inc.
    • 44911-0490 - Elimitone

NDC 44911-0490-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Elimitone with NDC 44911-0490 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Elimitone is bellis perennis, echinacea (angustifolia), trifolium pratense, phytolacca decandra, arnica montana, anas barbariae, hepatis et cordis extractum, calcarea iodata, kali muriaticum, nitricum acidum, phosphoricum acidum, sulphur iodatum. 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.


Elimitone 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.

  • BELLIS PERENNIS 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • ARNICA MONTANA 12 [hp_X]/mL
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 12 [hp_X]/mL
  • CALCIUM IODIDE 12 [hp_X]/mL
  • POTASSIUM CHLORIDE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • SULFUR IODIDE 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.

* Please review the disclaimer below.

Elimitone Product Label Images

Elimitone 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:

Bellis Perennis 3X, Echinacea (Angustifolia) 3X, Trifolium Pratense 3X, Phytolacca Decandra 4X, Arnica Montana 12X, Calcarea Iodata 12X, Kali Muriaticum 12X, Nitricum Acidum 12X, Anas Barbariae 12X, Phosphoricum Acidum 12X, Sulphur Iodatum 12X.

Indications:

May temporarily relieve swellings with heat and inflammation and sore throat irritation.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve swellings with heat and inflammation and sore throat irritation.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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.WARNING: Severe or persistent sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.

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 more than 2 days, 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   800.869.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYELIMITONE1 fl. oz. (30 ml)

* Please review the disclaimer below.

Previous Code
44911-0489
Next Code
44911-0491