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  4. NDC Product Code: 43742-2125 Bart Homo

NDC 43742-2125 Bart Homo

Bartonella Bacilliformis,Bartonella Bacilliformis Dna,Bartonella Clarridgeiae,Bartonella - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2125?
  4. Bart Homo Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
43742-2125
Proprietary Name:
Bart Homo
Non-Proprietary Name: [1]
Bartonella Bacilliformis, Bartonella Bacilliformis Dna, Bartonella Clarridgeiae, Bartonella Clarridgeiae Dna, Bartonella Elizabethae, Bartonella Henselae, Bartonella Henselae Dna, Bartonella Quintana, Bartonella Quintana Dna, Bartonella Vinsonii, Bartonella Vinsonii Dna, Bartonella Washoensis, Bartonella Washoensis Dna, Bartonella Elizabethae Dna
Substance Name: [2]
Bartonella Bacilliformis; Bartonella Bacilliformis Dna; Bartonella Clarridgeiae; Bartonella Clarridgeiae Dna; Bartonella Elizabethae; Bartonella Henselae; Bartonella Henselae Dna; Bartonella Quintana; Bartonella Quintana Dna; Bartonella Vinsonii; Bartonella Vinsonii Dna; Bartonella Washoensis; Bartonella Washoensis Dna; Herring Sperm Dna
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:
    f6b31232-aed0-469f-a4fa-ec5b9b45854f
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-08-2024
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43742-2125?

    The NDC code 43742-2125 is assigned by the FDA to the product Bart Homo which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bart Homo is bartonella bacilliformis, bartonella bacilliformis dna, bartonella clarridgeiae, bartonella clarridgeiae dna, bartonella elizabethae, bartonella henselae, bartonella henselae dna, bartonella quintana, bartonella quintana dna, bartonella vinsonii, bartonella vinsonii dna, bartonella washoensis, bartonella washoensis dna, bartonella elizabethae dna. 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 43742-2125-1 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 Bart Homo?

    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 Bart Homo 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.

    Which are Bart Homo UNII Codes?

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

    • BARTONELLA BACILLIFORMIS (UNII: FHE1Q0VN6P)
    • BARTONELLA BACILLIFORMIS (UNII: FHE1Q0VN6P) (Active Moiety)
    • BARTONELLA BACILLIFORMIS DNA (UNII: 738RYFW7B0)
    • BARTONELLA BACILLIFORMIS DNA (UNII: 738RYFW7B0) (Active Moiety)
    • BARTONELLA CLARRIDGEIAE (UNII: OZ0ND08BLR)
    • BARTONELLA CLARRIDGEIAE (UNII: OZ0ND08BLR) (Active Moiety)
    • BARTONELLA CLARRIDGEIAE DNA (UNII: 10AX0OV0LC)
    • BARTONELLA CLARRIDGEIAE DNA (UNII: 10AX0OV0LC) (Active Moiety)
    • BARTONELLA ELIZABETHAE (UNII: 437GVI6AH4)
    • BARTONELLA ELIZABETHAE (UNII: 437GVI6AH4) (Active Moiety)
    • BARTONELLA HENSELAE (UNII: 84PG7W9845)
    • BARTONELLA HENSELAE (UNII: 84PG7W9845) (Active Moiety)
    • BARTONELLA HENSELAE DNA (UNII: NG7PRUZQ2B)
    • BARTONELLA HENSELAE DNA (UNII: NG7PRUZQ2B) (Active Moiety)
    • BARTONELLA QUINTANA (UNII: 9R2271TA4J)
    • BARTONELLA QUINTANA (UNII: 9R2271TA4J) (Active Moiety)
    • BARTONELLA QUINTANA DNA (UNII: HLHV7DJTY8)
    • BARTONELLA QUINTANA DNA (UNII: HLHV7DJTY8) (Active Moiety)
    • BARTONELLA VINSONII (UNII: NF30MCQ9AC)
    • BARTONELLA VINSONII (UNII: NF30MCQ9AC) (Active Moiety)
    • BARTONELLA VINSONII DNA (UNII: 3PCT9PZ598)
    • BARTONELLA VINSONII DNA (UNII: 3PCT9PZ598) (Active Moiety)
    • BARTONELLA WASHOENSIS (UNII: 4040O0IM00)
    • BARTONELLA WASHOENSIS (UNII: 4040O0IM00) (Active Moiety)
    • BARTONELLA WASHOENSIS DNA (UNII: MYN27RGLNV)
    • BARTONELLA WASHOENSIS DNA (UNII: MYN27RGLNV) (Active Moiety)
    • HERRING SPERM DNA (UNII: 51FI676N6F)
    • HERRING SPERM DNA (UNII: 51FI676N6F) (Active Moiety)

    Which are Bart Homo 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:

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    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".