NDC 43742-0015 Biological Complex Iii

Anthracinum,Arsenicum Album,Botulinum,Calcarea Hypophosphorosa,Coxiella Burnetii,Dysentery - View Dosage, Usage, Ingredients, Routes, UNII

Product Information
Product Packages
What is NDC 43742-0015?
Biological Complex Iii Uses
Active Ingredients
Active Ingredients UNII Codes
Inactive Ingredients UNII Codes
Pharmacologic Classes

Product Information

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

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 Name: [5]

Deseret Biologicals, Inc.

Labeler Code:

43742

Product Label ID:

903c680c-c7fc-4671-b809-1b81bd4c6be4

Marketing Category: [8]

UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Start Marketing Date: [9]

04-26-2012

Listing Expiration Date: [11]

12-31-2024

Exclude Flag: [12]

Code Structure:

43742 - Deseret Biologicals, Inc.
- 43742-0015 - Biological Complex
  - 43742-0015-1

Code Navigator:

Product Packages

NDC Code 43742-0015-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 43742-0015?

The NDC code 43742-0015 is assigned by the FDA to the product Biological Complex Iii which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Biological Complex Iii is 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, . The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 43742-0015-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Biological Complex Iii?

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 Biological Complex Iii Active Ingredients?

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
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 Biological Complex Iii 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 Biological Complex Iii Inactive Ingredients 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 for Biological Complex Iii?

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 disclaimer below.

Product Footnotes

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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