Hp Axis Liquid
NDC 43742-1514

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1514?
  4. Hp Axis Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Hp Axis (argentum nitricum, berberis vulgaris, iodium, kali carbonicum, natrum muriaticum, adrenalinum, cortisone aceticum, dhea, glandula suprarenalis suis, hypophysis suis, hypothalamus suis, melatonin, testosterone, arsenicum album, phosphorus, proteus (vulgaris), sepia, silicea, alloxanum, corticotropin releasing hormone, adrenocorticotrophin, aldosterone) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a adrenergic alpha-agonists [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1514 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-1514
Proprietary Name:
Hp Axis
Non-Proprietary Name: [1]
Argentum Nitricum, Berberis Vulgaris, Iodium, Kali Carbonicum, Natrum Muriaticum, Adrenalinum, Cortisone Aceticum, Dhea, Glandula Suprarenalis Suis, Hypophysis Suis, Hypothalamus Suis, Melatonin, Testosterone, Arsenicum Album, Phosphorus, Proteus (vulgaris), Sepia, Silicea, Alloxanum, Corticotropin Releasing Hormone, Adrenocorticotrophin, Aldosterone
Substance Name: [2]
Aldosterone; Alloxan; Arsenic Trioxide; Berberis Vulgaris Root Bark; Corticorelin; Corticotropin; Cortisone Acetate; Epinephrine; Iodine; Melatonin; Phosphorus; Potassium Carbonate; Prasterone; Proteus Vulgaris; Sepia Officinalis Juice; Silicon Dioxide; Silver Nitrate; Sodium Chloride; Sus Scrofa Adrenal Gland; Sus Scrofa Hypothalamus; Sus Scrofa Pituitary Gland; Testosterone
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:
402f5b05-c71e-4dba-bc2b-049aee42952a
DEA Schedule: [7]
Schedule III (CIII) Substances
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-26-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-1514?

The NDC code 43742-1514 is assigned by the FDA to the product Hp Axis. It is commonly known by its generic name, argentum nitricum, berberis vulgaris, iodium, kali carbonicum, natrum muriaticum, adrenalinum, cortisone aceticum, dhea, glandula suprarenalis suis, hypophysis suis, hypothalamus suis, melatonin, testosterone, arsenicum album, phosphorus, proteus (vulgaris), sepia, silicea, alloxanum, corticotropin releasing hormone, adrenocorticotrophin, aldosterone. 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: 43742-1514-1. 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 temporary relief of symptoms related to circadian rhythm imbalances such as overuse of stimulants, anxiousness, sleep disturbances, circulatory imbalances, decreased sex drive and salt cravings.****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 circadian rhythm imbalances such as overuse of stimulants, anxiousness, sleep disturbances, circulatory imbalances, decreased sex drive and salt cravings.****These statements are based upon traditional 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.
  • ALDOSTERONE 15 [hp_C]/mL - A hormone secreted by the ADRENAL CORTEX that regulates electrolyte and water balance by increasing the renal retention of sodium and the excretion of potassium.
  • ALLOXAN 18 [hp_X]/mL - Acidic compound formed by oxidation of URIC ACID. It is isolated as an efflorescent crystalline hydrate.
  • ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
  • CORTICORELIN 12 [hp_C]/mL
  • CORTICOTROPIN 15 [hp_C]/mL
  • CORTISONE ACETATE 8 [hp_X]/mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
  • EPINEPHRINE 8 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
  • IODINE 6 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • MELATONIN 8 [hp_X]/mL - A biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.
  • PHOSPHORUS 12 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • POTASSIUM CARBONATE 6 [hp_X]/mL
  • PRASTERONE 8 [hp_X]/mL
  • PROTEUS VULGARIS 12 [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.
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
  • SILVER NITRATE 6 [hp_X]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
  • SODIUM CHLORIDE 6 [hp_X]/mL - A ubiquitous sodium salt that is commonly used to season food.
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 8 [hp_X]/mL
  • TESTOSTERONE 8 [hp_X]/mL - A potent androgenic steroid and major product secreted by the LEYDIG CELLS of the TESTIS. Its production is stimulated by LUTEINIZING HORMONE from the PITUITARY GLAND. In turn, testosterone exerts feedback control of the pituitary LH and FSH secretion. Depending on the tissues, testosterone can be further converted to DIHYDROTESTOSTERONE or ESTRADIOL.

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?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients 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 DEA Schedule? This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.
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".