NDC 43857-0024 Endocrine Balancer

Fucus Vesiculosus,Glycyrrhiza Glabra,Sarsaparilla,Glandula Suprarenalis Suis,Pinus - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43857-0024
Proprietary Name:
Endocrine Balancer
Non-Proprietary Name: [1]
Fucus Vesiculosus, Glycyrrhiza Glabra, Sarsaparilla, Glandula Suprarenalis Suis, Pinus Sylvestris, Thyroidinum (suis), Iodium
Substance Name: [2]
Fucus Vesiculosus; Glycyrrhiza Glabra; Iodine; Pinus Sylvestris Leafy Twig; Smilax Ornata Root; Sus Scrofa Adrenal Gland; Thyroid
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 Code:
    43857
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-14-2012
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 43857-0024?

    The NDC code 43857-0024 is assigned by the FDA to the product Endocrine Balancer which is a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Endocrine Balancer is fucus vesiculosus, glycyrrhiza glabra, sarsaparilla, glandula suprarenalis suis, pinus sylvestris, thyroidinum (suis), iodium. 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 43857-0024-1 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 Endocrine Balancer?

    For temporary relief of nervous exhaustion, mentally sluggish, easily fatigued, weak pulse, cold hands and feet and muscular exhaustion.  For temporary relief of nervous exhaustion, mentally sluggish, easily fatigues, weak pulse, cold hands and feet and muscular exhaustion.

    What are Endocrine Balancer 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.
    • 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.
    • GLYCYRRHIZA GLABRA 3 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
    • IODINE 12 [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.
    • PINUS SYLVESTRIS LEAFY TWIG 6 [hp_X]/mL
    • SMILAX ORNATA ROOT 3 [hp_X]/mL
    • SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL
    • THYROID 8 [hp_X]/mL - A highly vascularized endocrine gland consisting of two lobes joined by a thin band of tissue with one lobe on each side of the TRACHEA. It secretes THYROID HORMONES from the follicular cells and CALCITONIN from the parafollicular cells thereby regulating METABOLISM and CALCIUM level in blood, respectively.

    Which are Endocrine Balancer UNII Codes?

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

    Which are Endocrine Balancer 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 Endocrine Balancer?

    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 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.

    [11] 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.

    [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".