NDC 43742-1250 Allermilk

Taraxacum Officinale,Hydrastis Canadensis,Apiolum,Benzoicum Acidum,Cholinum,Cinnamic - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43742-1250
Proprietary Name:
Allermilk
Non-Proprietary Name: [1]
Taraxacum Officinale, Hydrastis Canadensis, Apiolum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Eugenol, Folic Acid, Histaminum Hydrochloricum, L-asparagine, Menadione, Octopamine, Oophorinum (suis), Phenyl Isothiocyanate, Piperine, Progesterone, Quercetin, Rutin, Saccharum Lactis, Vanillylamine, Xanthine, Coumarinum, Folliculinum, Formalinum, Gaba (gamma-aminobutyric Acid).
Substance Name: [2]
.gamma.-aminobutyric Acid; Apiole (parsley); Asparagine; Benzoic Acid; Choline Hydroxide; Cinnamic Acid; Coumarin; Estrone; Eugenol; Folic Acid; Formaldehyde; Goldenseal; Histamine Dihydrochloride; Lactose, Unspecified Form; Menadione; Octopamine Hydrochloride; Phenyl Isothiocyanate; Piperine; Progesterone; Quercetin; Rutin; Sus Scrofa Ovary; Taraxacum Officinale; Vanillylamine; Xanthine
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]
    11-09-2018
    End Marketing Date: [10]
    04-15-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-1250-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43742-1250?

    The NDC code 43742-1250 is assigned by the FDA to the product Allermilk which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Allermilk is taraxacum officinale, hydrastis canadensis, apiolum, benzoicum acidum, cholinum, cinnamic acid, eugenol, folic acid, histaminum hydrochloricum, l-asparagine, menadione, octopamine, oophorinum (suis), phenyl isothiocyanate, piperine, progesterone, quercetin, rutin, saccharum lactis, vanillylamine, xanthine, coumarinum, folliculinum, formalinum, gaba (gamma-aminobutyric acid).. 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 43742-1250-1 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 Allermilk?

    For the relief of symptoms related to sensitivity to milk or milk products including skin rash, hives, vomiting, bloating, cramping and occasional diarrhea.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the relief of symptoms related to sensitivity to milk or milk products including skin rash, hives, vomiting, bloating, cramping and occasional diarrhea.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Allermilk 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.
    • .GAMMA.-AMINOBUTYRIC ACID 8 [hp_X]/mL - The most common inhibitory neurotransmitter in the central nervous system.
    • APIOLE (PARSLEY) 6 [hp_X]/mL
    • ASPARAGINE 6 [hp_X]/mL - A non-essential amino acid that is involved in the metabolic control of cell functions in nerve and brain tissue. It is biosynthesized from ASPARTIC ACID and AMMONIA by asparagine synthetase. (From Concise Encyclopedia Biochemistry and Molecular Biology, 3rd ed)
    • BENZOIC ACID 6 [hp_X]/mL - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
    • CHOLINE HYDROXIDE 6 [hp_X]/mL - A basic constituent of lecithin that is found in many plants and animal organs. It is important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism.
    • CINNAMIC ACID 6 [hp_X]/mL
    • COUMARIN 8 [hp_X]/mL
    • ESTRONE 8 [hp_X]/mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
    • EUGENOL 6 [hp_X]/mL - A cinnamate derivative of the shikimate pathway found in CLOVE OIL and other PLANTS.
    • FOLIC ACID 6 [hp_X]/mL - A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.
    • FORMALDEHYDE 8 [hp_X]/mL - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
    • GOLDENSEAL 6 [hp_X]/mL
    • HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
    • LACTOSE, UNSPECIFIED FORM 6 [hp_X]/mL
    • MENADIONE 6 [hp_X]/mL
    • OCTOPAMINE HYDROCHLORIDE 6 [hp_X]/mL
    • PHENYL ISOTHIOCYANATE 6 [hp_X]/mL
    • PIPERINE 6 [hp_X]/mL
    • PROGESTERONE 6 [hp_X]/mL - The major progestational steroid that is secreted primarily by the CORPUS LUTEUM and the PLACENTA. Progesterone acts on the UTERUS, the MAMMARY GLANDS and the BRAIN. It is required in EMBRYO IMPLANTATION; PREGNANCY maintenance, and the development of mammary tissue for MILK production. Progesterone, converted from PREGNENOLONE, also serves as an intermediate in the biosynthesis of GONADAL STEROID HORMONES and adrenal CORTICOSTEROIDS.
    • QUERCETIN 6 [hp_X]/mL - A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin.
    • RUTIN 6 [hp_X]/mL - A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.
    • SUS SCROFA OVARY 6 [hp_X]/mL
    • TARAXACUM OFFICINALE 3 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
    • VANILLYLAMINE 6 [hp_X]/mL
    • XANTHINE 6 [hp_X]/mL - A purine base found in most body tissues and fluids, certain plants, and some urinary calculi. It is an intermediate in the degradation of adenosine monophosphate to uric acid, being formed by oxidation of hypoxanthine. The methylated xanthine compounds caffeine, theobromine, and theophylline and their derivatives are used in medicine for their bronchodilator effects. (Dorland, 28th ed)

    Which are Allermilk UNII Codes?

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

    Which are Allermilk 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 Allermilk?

    * 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".