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  4. NDC Product Code: 83014-0003 Weight Loss Support Plus Male Balance

NDC 83014-0003 Weight Loss Support Plus Male Balance

Agnus Castus,Foeniculum Vulgare,Ammonium Bromatum,Caladium Seguinum,Fucus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83014-0003?
  4. Weight Loss Support Plus Male Balance Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
83014-0003
Proprietary Name:
Weight Loss Support Plus Male Balance
Non-Proprietary Name: [1]
Agnus Castus, Foeniculum Vulgare, Ammonium Bromatum, Caladium Seguinum, Fucus Vesiculosus, Lecithin (derived From Egg), Capsicum Annuum, Galium Aparine, Hypothalamus Suis, Kali Bichromicum, Lac Defloratum (nspc), Phytolacca Decandra, Thyroidinum (bovine), Pituitarum Posterium (bovine), Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Selenium Metallicum, Adrenalinum, Phosphorus, Orchitinum (bovine), Onosmodium Virginianum
Substance Name: [2]
Ammonium Bromide; Antimony Trisulfide; Bos Taurus Pituitary Gland, Posterior; Bos Taurus Testicle; Capsicum; Chaste Tree Fruit; Dieffenbachia Seguine Whole; Egg Phospholipids; Epinephrine; Foeniculum Vulgare Fruit; Fucus Vesiculosus; Galium Aparine Whole; Onosmodium Virginianum; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Potassium Dichromate; Selenium; 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
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 Name: [5]
    Carolinas Weight Loss Institute
    Labeler Code:
    83014
    Product Label ID:
    3c983e80-4e58-4752-b70b-f7c1c2d1f724
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-10-2023
    End Marketing Date: [10]
    06-14-2028
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83014-0003?

    The NDC code 83014-0003 is assigned by the FDA to the product Weight Loss Support Plus Male Balance which is a human over the counter drug product labeled by Carolinas Weight Loss Institute. The generic name of Weight Loss Support Plus Male Balance is agnus castus, foeniculum vulgare, ammonium bromatum, caladium seguinum, fucus vesiculosus, lecithin (derived from egg), capsicum annuum, galium aparine, hypothalamus suis, kali bichromicum, lac defloratum (nspc), phytolacca decandra, thyroidinum (bovine), pituitarum posterium (bovine), antimonium crudum, argentum metallicum, calcarea carbonica, selenium metallicum, adrenalinum, phosphorus, orchitinum (bovine), onosmodium virginianum. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 83014-0003-1 60 ml in 1 bottle, spray . 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 Weight Loss Support Plus Male Balance?

    Adults: 3 to 5 sprays three to four times a day. Children under twelve, one half adult dosage. Consult a physician for use in children under 12 years of age. Do not take within 15 minutes of consuming food, beverage or brushing teeth.

    What are Weight Loss Support Plus Male Balance 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.

    Which are Weight Loss Support Plus Male Balance UNII Codes?

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

    Which are Weight Loss Support Plus Male Balance 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 Weight Loss Support Plus Male Balance?

    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.

    * 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".