Dysbio Plus Liquid
NDC 43742-2120

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2120?
  4. Dysbio Plus Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Dysbio Plus (aceticum acidum, aloe, arsenicum album, botulinum, brugia malayi, chininum sulphuricum, cholera nosode, clostridium difficile, colchicum autumnale, colibacillinum cum natrum muriaticum, colocynthis, echinacea (angustifolia), helicobacter pylori, helicobacter pylori dna, mercurius corrosivus, morgan gaertner, nux vomica, proteus (vulgaris), salmonella typhi nosode) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-2120 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-2120
Proprietary Name:
Dysbio Plus
Non-Proprietary Name: [1]
Aceticum Acidum, Aloe, Arsenicum Album, Botulinum, Brugia Malayi, Chininum Sulphuricum, Cholera Nosode, Clostridium Difficile, Colchicum Autumnale, Colibacillinum Cum Natrum Muriaticum, Colocynthis, Echinacea (angustifolia), Helicobacter Pylori, Helicobacter Pylori Dna, Mercurius Corrosivus, Morgan Gaertner, Nux Vomica, Proteus (vulgaris), Salmonella Typhi Nosode
Substance Name: [2]
Acetic Acid; Aloe; Arsenic Trioxide; Brugia Malayi; Citrullus Colocynthis Fruit Pulp; Clostridium Botulinum; Clostridium Difficile; Colchicum Autumnale Bulb; Echinacea Angustifolia Whole; Escherichia Coli; Helicobacter Pylori; Helicobacter Pylori Dna; Mercuric Chloride; Proteus Vulgaris; Quinine Sulfate; Salmonella Enterica Enterica Serovar Enteritidis; Salmonella Enterica Enterica Serovar Typhi; Strychnos Nux-vomica Seed; Vibrio Cholerae
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:
6864ab8e-3cf9-460e-b471-84ba3fb2efe0
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
02-07-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-2120?

The NDC code 43742-2120 is assigned by the FDA to the product Dysbio Plus. It is commonly known by its generic name, aceticum acidum, aloe, arsenicum album, botulinum, brugia malayi, chininum sulphuricum, cholera nosode, clostridium difficile, colchicum autumnale, colibacillinum cum natrum muriaticum, colocynthis, echinacea (angustifolia), helicobacter pylori, helicobacter pylori dna, mercurius corrosivus, morgan gaertner, nux vomica, proteus (vulgaris), salmonella typhi nosode. 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: 43742-2120-1. 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?

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.
  • ACETIC ACID 12 [hp_X]/mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
  • ALOE 7 [hp_X]/mL - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
  • ARSENIC TRIOXIDE 8 [hp_X]/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.
  • BRUGIA MALAYI 39 [hp_C]/mL - A species of parasitic nematode causing Malayan filariasis and having a distribution centering roughly on the Malay peninsula. The life cycle of B. malayi is similar to that of WUCHERERIA BANCROFTI, except that in most areas the principal mosquito vectors belong to the genus Mansonia.
  • CITRULLUS COLOCYNTHIS FRUIT PULP 8 [hp_X]/mL
  • CLOSTRIDIUM BOTULINUM 30 [hp_X]/mL - A species of anaerobic, gram-positive, rod-shaped bacteria in the family Clostridiaceae that produces proteins with characteristic neurotoxicity. It is the etiologic agent of BOTULISM in humans, wild fowl, HORSES; and CATTLE. Seven subtypes (sometimes called antigenic types, or strains) exist, each producing a different botulinum toxin (BOTULINUM TOXINS). The organism and its spores are widely distributed in nature.
  • CLOSTRIDIUM DIFFICILE 30 [hp_C]/mL
  • COLCHICUM AUTUMNALE BULB 8 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
  • ESCHERICHIA COLI 30 [hp_X]/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.
  • HELICOBACTER PYLORI 30 [hp_X]/mL - A spiral bacterium active as a human gastric pathogen. It is a gram-negative, urease-positive, curved or slightly spiral organism initially isolated in 1982 from patients with lesions of gastritis or peptic ulcers in Western Australia. Helicobacter pylori was originally classified in the genus CAMPYLOBACTER, but RNA sequencing, cellular fatty acid profiles, growth patterns, and other taxonomic characteristics indicate that the micro-organism should be included in the genus HELICOBACTER. It has been officially transferred to Helicobacter gen. nov. (see Int J Syst Bacteriol 1989 Oct;39(4):297-405).
  • HELICOBACTER PYLORI DNA 16 [hp_X]/mL
  • MERCURIC CHLORIDE 8 [hp_X]/mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
  • PROTEUS VULGARIS 16 [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.
  • QUININE SULFATE 12 [hp_X]/mL - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
  • SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI 33 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
  • VIBRIO CHOLERAE 16 [hp_X]/mL - The etiologic agent of CHOLERA.

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?

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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".