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  4. NDC Product Code: 43742-1528 Amoeba

NDC 43742-1528 Amoeba

Baptisia Tinctoria,Cajuputum,Capsicum Annuum,Fragaria Vesca,Hamamelis Virginiana,Quassia - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1528?
  4. Amoeba Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-1528
Proprietary Name:
Amoeba
Non-Proprietary Name: [1]
Baptisia Tinctoria, Cajuputum, Capsicum Annuum, Fragaria Vesca, Hamamelis Virginiana, Quassia (amara), Senna (cassia Angustifolia), Hydrastis Canadensis, Ipecacuanha, Hepar Suis, Pancreas Suis, Spleen (suis), Cinchona Officinalis, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Selenium Metallicum, Blastocystis Hominis, Cryptosporidium Parvum, Giardia Lamblia, Entamoeba Histolytica, Brugia Malayi
Substance Name: [2]
Alpine Strawberry; Baptisia Tinctoria Root; Blastocystis Hominis; Brugia Malayi; Cajuput Oil; Capsicum; Cinchona Officinalis Bark; Cryptosporidium Parvum; Entamoeba Histolytica; Giardia Lamblia; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Ipecac; Iridium; Lycopodium Clavatum Spore; Nitric Acid; Pork Liver; Quassia Amara Wood; Selenium; Senna Leaf; Strychnos Nux-vomica Seed; Sus Scrofa Pancreas; Sus Scrofa Spleen
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:
    dd4f5e44-1edf-44e0-8193-6f64bd00266a
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    08-21-2019
    End Marketing Date: [10]
    08-21-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43742-1528?

    The NDC code 43742-1528 is assigned by the FDA to the product Amoeba which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Amoeba is baptisia tinctoria, cajuputum, capsicum annuum, fragaria vesca, hamamelis virginiana, quassia (amara), senna (cassia angustifolia), hydrastis canadensis, ipecacuanha, hepar suis, pancreas suis, spleen (suis), cinchona officinalis, iridium metallicum, lycopodium clavatum, nitricum acidum, nux vomica, selenium metallicum, blastocystis hominis, cryptosporidium parvum, giardia lamblia, entamoeba histolytica, 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 43742-1528-1 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 Amoeba?

    For temporary relief of symptoms related to amoeba infestation including consequent weakness, fever, and stomach cramps.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to amoeba infestation including consequent weakness, fever, and stomach cramps.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Amoeba 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.
    • ALPINE STRAWBERRY 3 [hp_X]/mL - A plant genus of the family ROSACEAE known for the edible fruit.
    • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
    • BLASTOCYSTIS HOMINIS 12 [hp_C]/mL - A species of parasitic protozoa found in the intestines of humans and other primates. It was classified as a yeast in 1912. Over the years, questions arose about this designation. In 1967, many physiological and morphological B. hominis characteristics were reported that fit a protozoan classification. Since that time, other papers have corroborated this work and the organism is now recognized as a protozoan parasite of humans causing intestinal disease with potentially disabling symptoms.
    • 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.
    • CAJUPUT OIL 3 [hp_X]/mL
    • CAPSICUM 3 [hp_X]/mL - A plant genus of the family SOLANACEAE. The hot peppers yield CAPSAICIN, which activates VANILLOID RECEPTORS. Several varieties have sweet or pungent edible fruits that are used as vegetables when fresh and spices when the pods are dried.
    • CINCHONA OFFICINALIS BARK 12 [hp_X]/mL
    • CRYPTOSPORIDIUM PARVUM 12 [hp_C]/mL - A species of parasitic protozoa that infects humans and most domestic mammals. Its oocysts measure five microns in diameter. These organisms exhibit alternating cycles of sexual and asexual reproduction.
    • ENTAMOEBA HISTOLYTICA 18 [hp_C]/mL - A species of parasitic protozoa causing ENTAMOEBIASIS and amebic dysentery (DYSENTERY, AMEBIC). Characteristics include a single nucleus containing a small central karyosome and peripheral chromatin that is finely and regularly beaded.
    • GIARDIA LAMBLIA 12 [hp_C]/mL - A species of parasitic EUKARYOTES that attaches itself to the intestinal mucosa and feeds on mucous secretions. The organism is roughly pear-shaped and motility is somewhat erratic, with a slow oscillation about the long axis.
    • GOLDENSEAL 6 [hp_X]/mL
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X]/mL
    • IPECAC 6 [hp_X]/mL - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
    • IRIDIUM 12 [hp_X]/mL - A metallic element with the atomic symbol Ir, atomic number 77, and atomic weight 192.22.
    • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
    • NITRIC ACID 12 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
    • PORK LIVER 8 [hp_X]/mL
    • QUASSIA AMARA WOOD 3 [hp_X]/mL
    • SELENIUM 12 [hp_X]/mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
    • SENNA LEAF 3 [hp_X]/mL
    • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
    • SUS SCROFA PANCREAS 8 [hp_X]/mL
    • SUS SCROFA SPLEEN 8 [hp_X]/mL

    Which are Amoeba UNII Codes?

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

    Which are Amoeba 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".