Metabolic Correction Blend Spray
NDC 83073-0001

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 83073-0001?
  4. Metabolic Correction Blend Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Metabolic Correction Blend (foeniculum vulgare, ammonium bromatum, fucus vesiculosus, lecithin (derived from egg), capsicum annuum, galium aparine, hypothalamus suis, kali bichromicum, lac defloratum (nspc), phytolacca decandra, progesterone, thyroidinum (bovine), pituitarum posterium (bovine), antimonium crudum, argentum metallicum, calcarea carbonica, ferrum metallicum, graphites, adrenalinum, phosphorus) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Iha Distribution, Llc. This medication is typically used as a adrenergic alpha-agonists [moa]. It is supplied as a spray for oral administration. This product entry covers the primary NDC 83073-0001 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
83073-0001
Proprietary Name:
Metabolic Correction Blend
Non-Proprietary Name: [1]
Foeniculum Vulgare, Ammonium Bromatum, Fucus Vesiculosus, Lecithin (derived From Egg), Capsicum Annuum, Galium Aparine, Hypothalamus Suis, Kali Bichromicum, Lac Defloratum (nspc), Phytolacca Decandra, Progesterone, Thyroidinum (bovine), Pituitarum Posterium (bovine), Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Ferrum Metallicum, Graphites, Adrenalinum, Phosphorus
Substance Name: [2]
Ammonium Bromide; Antimony Trisulfide; Bos Taurus Pituitary Gland, Posterior; Capsicum; Egg Phospholipids; Epinephrine; Foeniculum Vulgare Fruit; Fucus Vesiculosus; Galium Aparine Whole; Graphite; Iron; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Potassium Dichromate; Progesterone; Silver; Skim Milk; Sus Scrofa Pituitary Gland; Thyroid, Bovine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Iha Distribution, Llc
Labeler Code:
83073
Product Label ID:
e8ec4f7e-c9dd-46dd-a9ee-2b8b7bcea9a8
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
03-21-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 83073-0001?

The NDC code 83073-0001 is assigned by the FDA to the product Metabolic Correction Blend. It is commonly known by its generic name, foeniculum vulgare, ammonium bromatum, fucus vesiculosus, lecithin (derived from egg), capsicum annuum, galium aparine, hypothalamus suis, kali bichromicum, lac defloratum (nspc), phytolacca decandra, progesterone, thyroidinum (bovine), pituitarum posterium (bovine), antimonium crudum, argentum metallicum, calcarea carbonica, ferrum metallicum, graphites, adrenalinum, phosphorus. This pharmaceutical product is labeled by Iha Distribution, Llc and is currently categorized as listed product. The medication is a spray administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 83073-0001-1. 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?

Adults use 4 sprays under the tongue three times daily or as directed by your Wellness Coach. Consult a physician for use in children under 12 years of age. Do not take within fifteen minutes of consuming food, beverages, or brushing teeth.

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.
  • AMMONIUM BROMIDE 3 [hp_X]/mL
  • ANTIMONY TRISULFIDE 9 [hp_X]/mL - structure given in first source
  • BOS TAURUS PITUITARY GLAND, POSTERIOR 8 [hp_X]/mL
  • CAPSICUM 6 [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.
  • EGG PHOSPHOLIPIDS 3 [hp_X]/mL
  • EPINEPHRINE 12 [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.
  • FOENICULUM VULGARE FRUIT 2 [hp_X]/mL
  • FUCUS VESICULOSUS 3 [hp_X]/mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
  • GALIUM APARINE WHOLE 6 [hp_X]/mL
  • GRAPHITE 9 [hp_X]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
  • IRON 9 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 9 [hp_X]/mL
  • 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.
  • PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
  • POTASSIUM DICHROMATE 6 [hp_X]/mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
  • 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.
  • SILVER 9 [hp_X]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
  • SKIM MILK 6 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL
  • THYROID, BOVINE 6 [hp_X]/mL

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 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".