Biological Complex Liquid
NDC 43742-0015
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Biological Complex (anthracinum, arsenicum album, botulinum, calcarea hypophosphorosa, coxiella burnetii, dysentery bacillus, francisella tularensis, gaertner bacillus, kali sulphuricum, lac caninum, malaria officinalis, mutabile bacillus, pertussinum, pestinum, pyrogenium, typhoid fever,) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a acetylcholine release inhibitor [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-0015 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
43742-0015
Proprietary Name:
Biological Complex Iii
Non-Proprietary Name: [1]
Anthracinum, Arsenicum Album, Botulinum, Calcarea Hypophosphorosa, Coxiella Burnetii, Dysentery Bacillus, Francisella Tularensis, Gaertner Bacillus, Kali Sulphuricum, Lac Caninum, Malaria Officinalis, Mutabile Bacillus, Pertussinum, Pestinum, Pyrogenium, Typhoid Fever,
Substance Name: [2]
Arsenic Trioxide; Bacillus Anthracis Immunoserum Rabbit; Botulinum Toxin Type A; Calcium Hypophosphite; Canis Lupus Familiaris Milk; Coxiella Burnetii; Escherichia Coli; Francisella Tularensis; Human Sputum, Bordetella Pertussis Infected; Plasmodium Malariae; Potassium Sulfate; Rancid Beef; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Salmonella Enterica Subsp. Enterica Serovar Typhi; Shigella Dysenteriae; Yersinia Pestis
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]
Labeler Code:
43742
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
04-26-2012
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 43742-0015?
The NDC code 43742-0015 is assigned by the FDA to the product Biological Complex Iii. It is commonly known by its generic name, anthracinum, arsenicum album, botulinum, calcarea hypophosphorosa, coxiella burnetii, dysentery bacillus, francisella tularensis, gaertner bacillus, kali sulphuricum, lac caninum, malaria officinalis, mutabile bacillus, pertussinum, pestinum, pyrogenium, typhoid fever, . 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. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-0015-1. 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?
For relief of symptoms related to systemic or cutaneous infection from specific biological substances; including headache, nausea, abdominal pain, chills, diarrhea, blurred vision, or food poisoning.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
For relief of symptoms related to systemic or cutaneous infection from specific biological substances; including headache, nausea, abdominal pain, chills, diarrhea, blurred vision, or food poisoning.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
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.
- ARSENIC TRIOXIDE 30 [hp_C]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 30 [hp_C]/mL
- BOTULINUM TOXIN TYPE A 30 [hp_C]/mL
- CALCIUM HYPOPHOSPHITE 30 [hp_C]/mL
- CANIS LUPUS FAMILIARIS MILK 30 [hp_C]/mL
- COXIELLA BURNETII 30 [hp_C]/mL - A species of gram-negative bacteria that grows preferentially in the vacuoles of the host cell. It is the etiological agent of Q FEVER.
- ESCHERICHIA COLI 30 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
- FRANCISELLA TULARENSIS 30 [hp_C]/mL - The etiologic agent of TULAREMIA in man and other warm-blooded animals.
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_C]/mL
- PLASMODIUM MALARIAE 30 [hp_C]/mL - A protozoan parasite that occurs primarily in subtropical and temperate areas. It is the causal agent of quartan malaria. As the parasite grows it exhibits little ameboid activity.
- POTASSIUM SULFATE 30 [hp_C]/mL - RN given refers to cpd with MF of K2-H2SO4
- RANCID BEEF 30 [hp_C]/mL
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI 30 [hp_C]/mL
- SHIGELLA DYSENTERIAE 30 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is extremely pathogenic and causes severe dysentery. Infection with this organism often leads to ulceration of the intestinal epithelium.
- YERSINIA PESTIS 30 [hp_C]/mL - The etiologic agent of PLAGUE in man, rats, ground squirrels, and other rodents.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694) (Active Moiety)
- CALCIUM HYPOPHOSPHITE (UNII: CUI83R2732)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- COXIELLA BURNETII (UNII: GRY5SDU86N)
- COXIELLA BURNETII (UNII: GRY5SDU86N) (Active Moiety)
- SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J)
- SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J) (Active Moiety)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H) (Active Moiety)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (Active Moiety)
- PLASMODIUM MALARIAE (UNII: AR76CST9I2)
- PLASMODIUM MALARIAE (UNII: AR76CST9I2) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (Active Moiety)
- YERSINIA PESTIS (UNII: S6JJH3XV1D)
- YERSINIA PESTIS (UNII: S6JJH3XV1D) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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.
- Acetylcholine Release Inhibitor - [EPC] (Established Pharmacologic Class)
- Acetylcholine Release Inhibitors - [MoA] (Mechanism of Action)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
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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".
