NDC 43742-2021 Dysbio Plus

Echinacea (angustifolia),Aloe,Colchicum Autumnale,Colocynthis,Mercurius Corrosivus,Nux - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43742-2021
Proprietary Name:
Dysbio Plus
Non-Proprietary Name: [1]
Echinacea (angustifolia), Aloe, Colchicum Autumnale, Colocynthis, Mercurius Corrosivus, Nux Vomica, Arsenicum Album, Aceticum Acidum, Chininum Sulphuricum, Cholera Nosode, Proteus (vulgaris), Colibacillinum Cum Natrum Muriaticum, Helicobacter Pylori, Botulinum, Salmonella Typhi Nosode, Morgan Gaertner, Clostridium Difficile, Brugia Malayi
Substance Name: [2]
Acetic Acid; Aloe; Arsenic Trioxide; Botulinum Toxin Type A; Brugia Malayi; Citrullus Colocynthis Fruit Pulp; Clostridium Difficile; Colchicum Autumnale Bulb; Echinacea Angustifolia Whole; Escherichia Coli; Helicobacter Pylori; Mercuric Chloride; Proteus Vulgaris; Quinine Sulfate; Salmonella Enterica Enterica Serovar Enteritidis; Salmonella Enterica Subsp. 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
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
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    06-28-2021
    End Marketing Date: [10]
    09-26-2027
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-2021-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43742-2021?

    The NDC code 43742-2021 is assigned by the FDA to the product Dysbio Plus which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Dysbio Plus is echinacea (angustifolia), aloe, colchicum autumnale, colocynthis, mercurius corrosivus, nux vomica, arsenicum album, aceticum acidum, chininum sulphuricum, cholera nosode, proteus (vulgaris), colibacillinum cum natrum muriaticum, helicobacter pylori, botulinum, salmonella typhi nosode, morgan gaertner, clostridium difficile, brugia malayi. 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 43742-2021-1 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 Dysbio Plus?

    For temporary relief of symptoms related to gastroenteritis including occasional diarrhea, stomach cramps, nausea, vomiting, flatulence and bloating.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to gastroenteritis including occasional diarrhea, stomach cramps, nausea, vomiting, flatulence and bloating.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Dysbio Plus 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.
    • 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.
    • BOTULINUM TOXIN TYPE A 30 [hp_X]/mL
    • 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 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).
    • 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 SUBSP. ENTERICA SEROVAR TYPHI 33 [hp_X]/mL
    • STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
    • VIBRIO CHOLERAE 12 [hp_X]/mL - The etiologic agent of CHOLERA.

    Which are Dysbio Plus UNII Codes?

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

    Which are Dysbio Plus 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:

    Which are the Pharmacologic Classes for Dysbio Plus?

    * 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.

    [10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

    [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".