NDC 43742-1587 Bacteria Combination

Adenosinum Triphosphoricum Dinatrum,Malicum Acidum,Natrum Oxalaceticum,Oroticum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43742-1587
Proprietary Name:
Bacteria Combination
Non-Proprietary Name: [1]
Adenosinum Triphosphoricum Dinatrum, Malicum Acidum, Natrum Oxalaceticum, Oroticum Acidum, Riboflavinum, Cinnamic Acid, Petroselinum Sativum, Colibacillinum Cum Natrum Muriaticum, Echinacea (angustifolia), Helicobacter Pylori, Mycoplasma Pneumoniae, Proteus (mirabilis), Proteus (vulgaris), Pseudomonas Aeruginosa, Salmonella Typhi Nosode, Enterococcus Faecalis, Streptococcus Mutans, Pneumococcinum, Streptococcus Agalactiae, Legionella Pneumophila, Listeria Monocytogenes, Dysentery Bacillus, Shigella Sonnei,
Substance Name: [2]
Adenosine Phosphate Disodium; Cinnamic Acid; Echinacea Angustifolia; Enterococcus Faecalis; Escherichia Coli; Helicobacter Pylori; Legionella Pneumophila; Listeria Monocytogenes; Malic Acid; Mycoplasma Pneumoniae; Orotic Acid Monohydrate; Petroselinum Crispum; Proteus Mirabilis; Proteus Morganii; Proteus Vulgaris; Pseudomonas Aeruginosa; Riboflavin; Salmonella Enterica Enterica Serovar Typhi; Shigella Dysenteriae; Shigella Sonnei; Sodium Diethyl Oxalacetate; Streptococcus Agalactiae; Streptococcus Dysgalactiae; Streptococcus Equinus; Streptococcus Mutans; Streptococcus Pneumoniae; Streptococcus Uberis; Streptococcus Viridans Group
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]
    11-18-2019
    End Marketing Date: [10]
    07-20-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-1587-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43742-1587?

    The NDC code 43742-1587 is assigned by the FDA to the product Bacteria Combination which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bacteria Combination is adenosinum triphosphoricum dinatrum, malicum acidum, natrum oxalaceticum, oroticum acidum, riboflavinum, cinnamic acid, petroselinum sativum, colibacillinum cum natrum muriaticum, echinacea (angustifolia), helicobacter pylori, mycoplasma pneumoniae, proteus (mirabilis), proteus (vulgaris), pseudomonas aeruginosa, salmonella typhi nosode, enterococcus faecalis, streptococcus mutans, pneumococcinum, streptococcus agalactiae, legionella pneumophila, listeria monocytogenes, dysentery bacillus, shigella sonnei, . 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 43742-1587-1 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 Bacteria Combination?

    For the temporary relief of symptoms related to common bacterial infections (respiratory and urinary tract infections, food poisoning) such as fever, headache, mucous congestion, stomach discomfort, cough, joint discomfort, and occasional diarrhea.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms related to common bacterial infections (respiratory and urinary tract infections, food poisoning) such as fever, headache, mucous congestion, stomach discomfort, cough, joint discomfort, and occasional diarrhea.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Bacteria Combination 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.
    • ADENOSINE PHOSPHATE DISODIUM 6 [hp_X]/mL - Adenine nucleotide containing one phosphate group esterified to the sugar moiety in the 2'-, 3'-, or 5'-position.
    • CINNAMIC ACID 6 [hp_X]/mL
    • ECHINACEA ANGUSTIFOLIA 15 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
    • ENTEROCOCCUS FAECALIS 13 [hp_C]/mL - A species of gram-positive, coccoid bacteria commonly isolated from clinical specimens and the human intestinal tract. Most strains are nonhemolytic.
    • ESCHERICHIA COLI 15 [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 15 [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).
    • LEGIONELLA PNEUMOPHILA 14 [hp_C]/mL - A species of gram-negative, aerobic bacteria that is the causative agent of LEGIONNAIRES' DISEASE. It has been isolated from numerous environmental sites as well as from human lung tissue, respiratory secretions, and blood.
    • LISTERIA MONOCYTOGENES 14 [hp_C]/mL - A species of gram-positive, rod-shaped bacteria widely distributed in nature. It has been isolated from sewage, soil, silage, and from feces of healthy animals and man. Infection with this bacterium leads to encephalitis, meningitis, endocarditis, and abortion.
    • MALIC ACID 6 [hp_X]/mL
    • MYCOPLASMA PNEUMONIAE 15 [hp_X]/mL - Short filamentous organism of the genus Mycoplasma, which binds firmly to the cells of the respiratory epithelium. It is one of the etiologic agents of non-viral primary atypical pneumonia in man.
    • OROTIC ACID MONOHYDRATE 6 [hp_X]/mL
    • PETROSELINUM CRISPUM 6 [hp_X]/mL - A plant genus of the family APIACEAE used for flavoring food.
    • PROTEUS MIRABILIS 15 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is frequently isolated from clinical specimens. Its most common site of infection is the urinary tract.
    • PROTEUS MORGANII 30 [hp_C]/mL
    • PROTEUS VULGARIS 15 [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.
    • PSEUDOMONAS AERUGINOSA 15 [hp_X]/mL - A species of gram-negative, aerobic, rod-shaped bacteria commonly isolated from clinical specimens (wound, burn, and urinary tract infections). It is also found widely distributed in soil and water. P. aeruginosa is a major agent of nosocomial infection.
    • RIBOFLAVIN 6 [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.
    • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI 17 [hp_X]/mL
    • SHIGELLA DYSENTERIAE 15 [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.
    • SHIGELLA SONNEI 15 [hp_C]/mL - A lactose-fermenting bacterium causing dysentery.
    • SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
    • STREPTOCOCCUS AGALACTIAE 14 [hp_C]/mL - A bacterium which causes mastitis in cattle and occasionally in man.
    • STREPTOCOCCUS DYSGALACTIAE 15 [hp_C]/mL
    • STREPTOCOCCUS EQUINUS 15 [hp_C]/mL - A species of gram-positive, coccoid bacteria commonly found in the alimentary tract of cows, sheep, and other ruminants. It occasionally is encountered in cases of human endocarditis. This species is nonhemolytic.
    • STREPTOCOCCUS MUTANS 13 [hp_C]/mL - A polysaccharide-producing species of STREPTOCOCCUS isolated from human dental plaque.
    • STREPTOCOCCUS PNEUMONIAE 13 [hp_C]/mL - A gram-positive organism found in the upper respiratory tract, inflammatory exudates, and various body fluids of normal and/or diseased humans and, rarely, domestic animals.
    • STREPTOCOCCUS UBERIS 32 [hp_C]/mL
    • STREPTOCOCCUS VIRIDANS GROUP 38 [hp_C]/mL

    Which are Bacteria Combination UNII Codes?

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

    Which are Bacteria Combination 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:

    * 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".