NDC 44911-0266 Pituistat

Aralia Quinquefolia, Ginkgo Biloba, Arsenicum Iodatum, Avena Sativa, Baryta Carbonica, Phosphorus, Silicea, Thyroidinum (suis), Aluminum, Antimony, Barium, Beryllium, Bismuth, Boron, Bromine, Calcium, Carbon, Cerium, Cesium, Chloride, Chromium, Cobalt, Copper, Dysprosium, Erbium, Europium, Fluoride, Gadolinium, Gallium, Germanium, Gold, Hafnium, Holmium, Indium, Iodine, Iridium, Iron, Lanthanum, Lithium, Lutetium, Magnesium, Manganese, Molybdenum, Neodymium, Nickel, Niobium, Osmium, Palladium

NDC Product Code 44911-0266

NDC Code: 44911-0266

Proprietary Name: Pituistat 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 Quinquefolia, Ginkgo Biloba, Arsenicum Iodatum, Avena Sativa, Baryta Carbonica, Phosphorus, Silicea, Thyroidinum (suis), Aluminum, Antimony, Barium, Beryllium, Bismuth, Boron, Bromine, Calcium, Carbon, Cerium, Cesium, Chloride, Chromium, Cobalt, Copper, Dysprosium, Erbium, Europium, Fluoride, Gadolinium, Gallium, Germanium, Gold, Hafnium, Holmium, Indium, Iodine, Iridium, Iron, Lanthanum, Lithium, Lutetium, Magnesium, Manganese, Molybdenum, Neodymium, Nickel, Niobium, Osmium, Palladium 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.

NDC 44911-0266-1

Package Description: 50 mL in 1 PACKAGE

NDC Product Information

Pituistat with NDC 44911-0266 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Pituistat is aralia quinquefolia, ginkgo biloba, arsenicum iodatum, avena sativa, baryta carbonica, phosphorus, silicea, thyroidinum (suis), aluminum, antimony, barium, beryllium, bismuth, boron, bromine, calcium, carbon, cerium, cesium, chloride, chromium, cobalt, copper, dysprosium, erbium, europium, fluoride, gadolinium, gallium, germanium, gold, hafnium, holmium, indium, iodine, iridium, iron, lanthanum, lithium, lutetium, magnesium, manganese, molybdenum, neodymium, nickel, niobium, osmium, palladium. 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.

Pituistat 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.

  • AMERICAN GINSENG 3 [hp_X]/mL
  • GINKGO 3 [hp_X]/mL
  • ARSENIC TRIIODIDE 12 [hp_X]/mL
  • AVENA SATIVA FLOWERING TOP 12 [hp_X]/mL
  • BARIUM CARBONATE 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL
  • THYROID, PORCINE 12 [hp_X]/mL
  • ALUMINUM 12 [hp_X]/mL
  • ANTIMONY 12 [hp_X]/mL
  • BARIUM 12 [hp_X]/mL
  • BERYLLIUM 12 [hp_X]/mL
  • BISMUTH 12 [hp_X]/mL
  • BORON 12 [hp_X]/mL
  • BROMINE 12 [hp_X]/mL
  • CALCIUM 12 [hp_X]/mL
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • CERIUM 12 [hp_X]/mL
  • CESIUM 12 [hp_X]/mL
  • CHLORIDE ION 12 [hp_X]/mL
  • CHROMIUM 12 [hp_X]/mL
  • COBALT 12 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • DYSPROSIUM 12 [hp_X]/mL
  • ERBIUM 12 [hp_X]/mL
  • EUROPIUM 12 [hp_X]/mL
  • FLUORIDE ION 12 [hp_X]/mL
  • GADOLINIUM 12 [hp_X]/mL
  • GALLIUM 12 [hp_X]/mL
  • GERMANIUM 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • HAFNIUM 12 [hp_X]/mL
  • HOLMIUM 12 [hp_X]/mL
  • INDIUM 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • IRIDIUM 12 [hp_X]/mL
  • IRON 12 [hp_X]/mL
  • LANTHANUM 12 [hp_X]/mL
  • LITHIUM 12 [hp_X]/mL
  • LUTETIUM 12 [hp_X]/mL
  • MAGNESIUM 12 [hp_X]/mL
  • MANGANESE 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • NEODYMIUM 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • NIOBIUM 12 [hp_X]/mL
  • OSMIUM 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • PLATINUM 12 [hp_X]/mL
  • POTASSIUM 12 [hp_X]/mL
  • PRASEODYMIUM 12 [hp_X]/mL
  • RHENIUM 12 [hp_X]/mL
  • RHODIUM 12 [hp_X]/mL
  • RUBIDIUM 12 [hp_X]/mL
  • RUTHENIUM 12 [hp_X]/mL
  • SAMARIUM 12 [hp_X]/mL
  • SCANDIUM 12 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • SILICON 12 [hp_X]/mL
  • SILVER 12 [hp_X]/mL
  • SODIUM 12 [hp_X]/mL
  • STRONTIUM 12 [hp_X]/mL
  • SULFUR 12 [hp_X]/mL
  • TANTALUM 12 [hp_X]/mL
  • TELLURIUM 12 [hp_X]/mL
  • TERBIUM 12 [hp_X]/mL
  • THALLIUM 12 [hp_X]/mL
  • THORIUM 12 [hp_X]/mL
  • THULIUM 12 [hp_X]/mL
  • TIN 12 [hp_X]/mL
  • TITANIUM 12 [hp_X]/mL
  • TUNGSTEN 12 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL
  • YTTERBIUM 12 [hp_X]/mL
  • YTTRIUM 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL
  • ZIRCONIUM 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: 09-24-2015 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: 12-31-2019 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.

Pituistat Product Label Images

Pituistat 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 Quinquefolia 3X, Ginkgo Biloba 3X, Arsenicum Iodatum 12X, Avena Sativa 12X, Baryta Carbonica 12X, Phosphorus 12X, Silicea 12X, Thyroidinum (Suis) 12X, Aluminum, Antimony, Barium, Beryllium, Bismuth, Boron, Bromine, Calcium, Carbon, Cerium, Cesium, Chloride, Chromium, Cobalt, Copper, Dysprosium, Erbium, Europium, Fluoride, Gadolinium, Gallium, Germanium, Gold, Hafnium, Holmium, Indium, Iodine, Iridium, Iron, Lanthanum, Lithium, Lutetium, Magnesium, Manganese, Molybdenum, Neodymium, Nickel, Niobium, Osmium, Palladium, Phosphorus, Platinum, Potassium, Praseodymium, Rhenium, Rhodium, Rubidium, Ruthenium, Samarium, Scandium, Selenium, Silicon, Silver, Sodium, Strontium, Sulfur, Tantalum, Tellurium, Terbium, Thallium, Thorium, Thulium, Tin, Titanium, Tungsten, Vanadium, Ytterbium, Yttrium, Zinc, Zirconium 12X, 30X.

Indications:

For temporary relief of mental sluggishness, confusion, weakness, lethargy, thirst and frequent urination.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For temporary relief of mental sluggishness, confusion, weakness, lethargy, thirst and frequent urination.****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 Blvd.Woodbine, IA 51579   800.869.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYPITUISTAT1.69 fl. oz. (20 ml)

* Please review the disclaimer below.