Allermilk Liquid
NDC 43742-1591

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1591?
  4. Allermilk Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Allermilk (taraxacum officinale, hydrastis canadensis, benzoicum acidum, cholinum, cinnamic acid, eugenol, folic acid, histaminum hydrochloricum, l-asparagine (monohydrate), menadione, oophorinum (suis), phenyl isothiocyanate, piperine, progesterone, quercetin, rutin, saccharum lactis, tyramine, xanthine, coumarinum, folliculinum, formalinum, gaba (gamma-aminobutyric acid), vanillylamine, apiolum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1591 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-1591
Proprietary Name:
Allermilk
Non-Proprietary Name: [1]
Taraxacum Officinale, Hydrastis Canadensis, Benzoicum Acidum, Cholinum, Cinnamic Acid, Eugenol, Folic Acid, Histaminum Hydrochloricum, L-asparagine (monohydrate), Menadione, Oophorinum (suis), Phenyl Isothiocyanate, Piperine, Progesterone, Quercetin, Rutin, Saccharum Lactis, Tyramine, Xanthine, Coumarinum, Folliculinum, Formalinum, Gaba (gamma-aminobutyric Acid), Vanillylamine, Apiolum
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; Phenyl Isothiocyanate; Piperine; Progesterone; Quercetin; Rutin; Sus Scrofa Ovary; Taraxacum Officinale; Tyramine; Vanillylamine; Xanthine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
c13cbfb9-1c1f-43b5-b218-e58c3c521f93
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
11-21-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-1591?

The NDC code 43742-1591 is assigned by the FDA to the product Allermilk. It is commonly known by its generic name, taraxacum officinale, hydrastis canadensis, benzoicum acidum, cholinum, cinnamic acid, eugenol, folic acid, histaminum hydrochloricum, l-asparagine (monohydrate), menadione, oophorinum (suis), phenyl isothiocyanate, piperine, progesterone, quercetin, rutin, saccharum lactis, tyramine, xanthine, coumarinum, folliculinum, formalinum, gaba (gamma-aminobutyric acid), vanillylamine, apiolum. This pharmaceutical product is labeled by Deseret Biologicals, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-1591-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 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 homeopathic principles. They have not been reviewed by the Food and Drug Administration.

What are Active Ingredients of this product?

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) 15 [hp_C]/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 - Synthetic or naturally occurring substances related to coumarin, the delta-lactone of coumarinic acid.
  • 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
  • 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.
  • TYRAMINE 6 [hp_X]/mL - An indirect sympathomimetic that occurs naturally in cheese and other foods. Tyramine does not directly activate adrenergic receptors, but it can serve as a substrate for adrenergic uptake systems and MONOAMINE OXIDASE to prolong the actions of adrenergic transmitters. It also provokes transmitter release from adrenergic terminals and may be a neurotransmitter in some invertebrate nervous systems.
  • VANILLYLAMINE 16 [hp_X]/mL - inhibits microsomal enzyme function; RN given refers to parent cpd; structure
  • XANTHINE 6 [hp_X]/mL - Purine bases found in body tissues and fluids and in some plants.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 of this product?

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".