Set 4te Homo Liquid
NDC 43742-2552

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2552?
  4. Set 4te Homo Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

This code was recently added to the official NDC directory and the product has entered commercial distribution.

Set 4te Homo (adeps suillus, bryonia (alba), calcarea phosphorica, cholinum, dna, dopamine (hydrochloride), ferrum phosphoricum, folic acid, insulinum (human), leptin, magnesia muriatica, l-methionine, methylcobalamin, proteus (vulgaris), rhus tox, riboflavinum, ruta graveolens, saccharum officinale, thiosinaminum, zincum metallicum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a blood coagulation factor [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-2552 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-2552
Proprietary Name:
Set 4te Homo
Non-Proprietary Name: [1]
Adeps Suillus, Bryonia (alba), Calcarea Phosphorica, Cholinum, Dna, Dopamine (hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum (human), Leptin, Magnesia Muriatica, L-methionine, Methylcobalamin, Proteus (vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum
Substance Name: [2]
Allylthiourea; Bryonia Alba Root; Choline Hydroxide; Dopamine Hydrochloride; Ferrosoferric Phosphate; Folic Acid; Herring Sperm Dna; Insulin Human; Lard; Leptin Human; Magnesium Chloride; Methionine; Methylcobalamin; Proteus Vulgaris; Riboflavin; Ruta Graveolens Flowering Top; Sucrose; Toxicodendron Pubescens Leaf; Tribasic Calcium Phosphate; 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]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
e7b8d75b-f2bc-4013-91e7-bf5bbec11a90
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
06-25-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-2552?

The NDC code 43742-2552 is assigned by the FDA to the product Set 4te Homo. It is commonly known by its generic name, adeps suillus, bryonia (alba), calcarea phosphorica, cholinum, dna, dopamine (hydrochloride), ferrum phosphoricum, folic acid, insulinum (human), leptin, magnesia muriatica, l-methionine, methylcobalamin, proteus (vulgaris), rhus tox, riboflavinum, ruta graveolens, saccharum officinale, thiosinaminum, zincum metallicum. This pharmaceutical product is labeled by Deseret Biologicals, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. 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?

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

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.
  • ALLYLTHIOUREA 9 [hp_X]/mL
  • BRYONIA ALBA ROOT 9 [hp_X]/mL
  • CHOLINE HYDROXIDE 9 [hp_X]/mL - A basic constituent of lecithin that is found in many plants and animal organs. It is important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism.
  • DOPAMINE HYDROCHLORIDE 9 [hp_X]/mL - One of the catecholamine NEUROTRANSMITTERS in the brain. It is derived from TYROSINE and is the precursor to NOREPINEPHRINE and EPINEPHRINE. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (RECEPTORS, DOPAMINE) mediate its action.
  • FERROSOFERRIC PHOSPHATE 9 [hp_X]/mL
  • FOLIC ACID 9 [hp_X]/mL - A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.
  • HERRING SPERM DNA 9 [hp_X]/mL
  • INSULIN HUMAN 9 [hp_X]/mL
  • LARD 9 [hp_X]/mL
  • LEPTIN HUMAN 9 [hp_X]/mL
  • MAGNESIUM CHLORIDE 9 [hp_X]/mL - Magnesium chloride. An inorganic compound consisting of one magnesium and two chloride ions. The compound is used in medicine as a source of magnesium ions, which are essential for many cellular activities. It has also been used as a cathartic and in alloys.
  • METHIONINE 9 [hp_X]/mL - A sulfur-containing essential L-amino acid that is important in many body functions.
  • METHYLCOBALAMIN 9 [hp_X]/mL
  • PROTEUS VULGARIS 12 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
  • RIBOFLAVIN 9 [hp_X]/mL - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
  • RUTA GRAVEOLENS FLOWERING TOP 9 [hp_X]/mL
  • SUCROSE 9 [hp_X]/mL - A nonreducing disaccharide composed of GLUCOSE and FRUCTOSE linked via their anomeric carbons. It is obtained commercially from SUGARCANE, sugar beet (BETA VULGARIS), and other plants and used extensively as a food and a sweetener.
  • TOXICODENDRON PUBESCENS LEAF 9 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 9 [hp_X]/mL
  • ZINC 9 [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.

* Please review the full disclaimer at the bottom of this page.

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".