NDC 73162-0001 Fat Loss Activation Complex

Fucus Vesiculosus,Kali Carbonicum,Agave Americana,Capsicum Annuum,Phytolacca - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
73162-0001
Proprietary Name:
Fat Loss Activation Complex
Non-Proprietary Name: [1]
Fucus Vesiculosus, Kali Carbonicum, Agave Americana, Capsicum Annuum, Phytolacca Decandra, Aurum Metallicum, Calcarea Carbonica, Ferrum Metallicum, Graphites
Substance Name: [2]
Agave Americana Leaf; Capsicum; Fucus Vesiculosus; Gold; Graphite; Iron; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Potassium Carbonate
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]
    Health Masters Llc
    Labeler Code:
    73162
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-26-2020
    End Marketing Date: [10]
    02-26-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 73162-0001-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 73162-0001?

    The NDC code 73162-0001 is assigned by the FDA to the product Fat Loss Activation Complex which is a human over the counter drug product labeled by Health Masters Llc. The generic name of Fat Loss Activation Complex is fucus vesiculosus, kali carbonicum, agave americana, capsicum annuum, phytolacca decandra, aurum metallicum, calcarea carbonica, ferrum metallicum, graphites. 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 73162-0001-1 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 Fat Loss Activation Complex?

    For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache, fatigue and detoxification stress. For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache, fatigue and detoxification stress.

    What are Fat Loss Activation Complex 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.
    • AGAVE AMERICANA LEAF 4 [hp_X]/mL
    • CAPSICUM 4 [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.
    • FUCUS VESICULOSUS 2 [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.
    • GOLD 8 [hp_X]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
    • GRAPHITE 8 [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 8 [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 8 [hp_X]/mL
    • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
    • POTASSIUM CARBONATE 2 [hp_X]/mL

    Which are Fat Loss Activation Complex UNII Codes?

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

    Which are Fat Loss Activation Complex 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 Fat Loss Activation Complex?

    * 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".