NDC 44911-0449 Systemistat

Berberis Vulgaris, Chelidonium Majus, Lappa Major, Hydrastis Canadensis, Hepar Sulphuris Calcareum, Lycopodium Clavatum, Sulphur, Calcarea Carbonica, Mercurius Solubilis, Thuja Occidentalis

NDC Product Code 44911-0449

NDC Code: 44911-0449

Proprietary Name: Systemistat 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: Berberis Vulgaris, Chelidonium Majus, Lappa Major, Hydrastis Canadensis, Hepar Sulphuris Calcareum, Lycopodium Clavatum, Sulphur, Calcarea Carbonica, Mercurius Solubilis, Thuja Occidentalis 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.
    • 44911-0449 - Systemistat

NDC 44911-0449-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Systemistat with NDC 44911-0449 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Systemistat is berberis vulgaris, chelidonium majus, lappa major, hydrastis canadensis, hepar sulphuris calcareum, lycopodium clavatum, sulphur, calcarea carbonica, mercurius solubilis, thuja occidentalis. 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.


Systemistat 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.

  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • CALCIUM SULFIDE 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • SULFUR 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
  • MERCURIUS SOLUBILIS 30 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 30 [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.

Systemistat Product Label Images

Systemistat 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:

Berberis Vulgaris 3X, Chelidonium Majus 3X,  Lappa Major 3X, Hydrastis Canadensis 5X, Hepar Sulphuris Calcareum 12X, Lycopodium Clavatum 12X, Sulphur 12X, Calcarea Carbonica 30X, Mercurius Solubilis 30X, Thuja Occidentalis 30X.

Indications:

May temporarily relieve painless, clay colored diarrhea, eczema with itching, and burning hay fever with offensive discharge running from the nose.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve painless, clay colored diarrhea, eczema with itching, and burning hay fever with offensive discharge running from the nose.****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.

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 1987HOMEPATHIC REMEDYSYSTEMISTAT1 fl. oz. (30 ml)

* Please review the disclaimer below.

Previous Code
44911-0448
Next Code
44911-0450