Spleenex Liquid
NDC 44911-0294

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0294?
  4. Spleenex VH Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Spleenex (aralia quinquefolia, ginkgo biloba, pancreas suis, spleen (suis), stomach (suis), germanium sesquioxide, cobaltum metallicum, niccolum metallicum, zincum metallicum, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malic acid, pyruvic acid, succinicum acidum, naphthoquinone, baryta carbonica, phosphoricum acidum, aconiticum acidum, cis, magnesium gluconicum dihydricum, nux vomica, phosphorus) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energique, Inc.. This medication is typically used as a acidifying activity [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 44911-0294 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0294
Proprietary Name:
Spleenex VH
Non-Proprietary Name: [1]
Aralia Quinquefolia, Ginkgo Biloba, Pancreas Suis, Spleen (suis), Stomach (suis), Germanium Sesquioxide, Cobaltum Metallicum, Niccolum Metallicum, Zincum Metallicum, Alpha-ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malic Acid, Pyruvic Acid, Succinicum Acidum, Naphthoquinone, Baryta Carbonica, Phosphoricum Acidum, Aconiticum Acidum, Cis, Magnesium Gluconicum Dihydricum, Nux Vomica, Phosphorus
Substance Name: [2]
Aconitic Acid, (z)-; American Ginseng; Anhydrous Citric Acid; Barium Carbonate; Cobalt; Fumaric Acid; Germanium Sesquioxide; Ginkgo; Magnesium Gluconate; Malic Acid; Naphthoquine; Nickel; Oxogluric Acid; Phosphoric Acid; Phosphorus; Pyruvic Acid; Strychnos Nux-vomica Seed; Succinic Acid; Sus Scrofa Pancreas; Sus Scrofa Spleen; Sus Scrofa Stomach; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
54e2c88e-2483-4c38-86e5-19e218e713ae
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
11-11-2015
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 44911-0294?

The NDC code 44911-0294 is assigned by the FDA to the product Spleenex VH. It is commonly known by its generic name, aralia quinquefolia, ginkgo biloba, pancreas suis, spleen (suis), stomach (suis), germanium sesquioxide, cobaltum metallicum, niccolum metallicum, zincum metallicum, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malic acid, pyruvic acid, succinicum acidum, naphthoquinone, baryta carbonica, phosphoricum acidum, aconiticum acidum, cis, magnesium gluconicum dihydricum, nux vomica, phosphorus. This pharmaceutical product is labeled by Energique, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 44911-0294-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

May temporarily relieve heaviness and fullness after eating little, stomach pain, and weak digestion.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve heaviness and fullness after eating little, stomach pain, weak digestion.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

What are Active Ingredients of this product?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ACONITIC ACID, (Z)- 12 [hp_X]/mL
  • AMERICAN GINSENG 3 [hp_X]/mL
  • ANHYDROUS CITRIC ACID 8 [hp_X]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
  • BARIUM CARBONATE 12 [hp_X]/mL
  • COBALT 8 [hp_X]/mL - A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis.
  • FUMARIC ACID 8 [hp_X]/mL - see also record for ferrous fumarate; use FUMARATES for general fumaric acid esters
  • GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
  • GINKGO 6 [hp_X]/mL - The only specie of the genus Ginkgo, family Ginkgoacea. It is the source of extracts of medicinal interest, especially Egb 761. Ginkgo may refer to the genus or species.
  • MAGNESIUM GLUCONATE 12 [hp_X]/mL
  • MALIC ACID 8 [hp_X]/mL
  • NAPHTHOQUINE 9 [hp_X]/mL - has antimalarial activity
  • NICKEL 8 [hp_X]/mL - A trace element with the atomic symbol Ni, atomic number 28, and atomic weight 58.69. It is a cofactor of the enzyme UREASE.
  • OXOGLURIC ACID 8 [hp_X]/mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
  • PHOSPHORIC ACID 12 [hp_X]/mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • PHOSPHORUS 12 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • PYRUVIC ACID 8 [hp_X]/mL - An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • SUCCINIC ACID 8 [hp_X]/mL - A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
  • SUS SCROFA PANCREAS 6 [hp_X]/mL
  • SUS SCROFA SPLEEN 6 [hp_X]/mL
  • SUS SCROFA STOMACH 6 [hp_X]/mL
  • ZINC 8 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
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.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".