Weight Loss Support Plus Female Balance Spray
NDC 83014-0008

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 83014-0008?
  4. Weight Loss Support Plus Female Balance Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Weight Loss Support Plus Female Balance (foeniculum vulgare, ammonium bromatum, fucus vesiculosus, lecithin (derived from egg), capsicum annuum, caulophyllum thalictrines, cimicifuga racemosa, galium aparine, hypothalamus suis, kali bichromicum, lac defloratum, phytolacca decandra, rubus idaeus, thyroidinum (bovine), pituitarum posterium (bovine), antimonium crudum, argentum metallicum, calcarea carbonica, adrenalinum, phosphorus, hepar sulphuris calcareum, progesterone, oxytocin) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Carolinas Weight Loss Institute. 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 83014-0008 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
83014-0008
Proprietary Name:
Weight Loss Support Plus Female Balance
Non-Proprietary Name: [1]
Foeniculum Vulgare, Ammonium Bromatum, Fucus Vesiculosus, Lecithin (derived From Egg), Capsicum Annuum, Caulophyllum Thalictrines, Cimicifuga Racemosa, Galium Aparine, Hypothalamus Suis, Kali Bichromicum, Lac Defloratum, Phytolacca Decandra, Rubus Idaeus, Thyroidinum (bovine), Pituitarum Posterium (bovine), Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Adrenalinum, Phosphorus, Hepar Sulphuris Calcareum, Progesterone, Oxytocin
Substance Name: [2]
Ammonium Bromide; Antimony Trisulfide; Black Cohosh; Bos Taurus Pituitary Gland, Posterior; Calcium Sulfide; Capsicum; Caulophyllum Thalictroides Root; Egg Phospholipids; Epinephrine; Foeniculum Vulgare Fruit; Fucus Vesiculosus; Galium Aparine Whole; Oxytocin; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Potassium Dichromate; Progesterone; Rubus Idaeus Leaf; Silver; Skim Milk; Sus Scrofa Hypothalamus; 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]
Carolinas Weight Loss Institute
Labeler Code:
83014
Product Label ID:
66249339-1e80-449f-9c2a-a030cdc71a0c
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-23-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 83014-0008?

The NDC code 83014-0008 is assigned by the FDA to the product Weight Loss Support Plus Female Balance. It is commonly known by its generic name, foeniculum vulgare, ammonium bromatum, fucus vesiculosus, lecithin (derived from egg), capsicum annuum, caulophyllum thalictrines, cimicifuga racemosa, galium aparine, hypothalamus suis, kali bichromicum, lac defloratum, phytolacca decandra, rubus idaeus, thyroidinum (bovine), pituitarum posterium (bovine), antimonium crudum, argentum metallicum, calcarea carbonica, adrenalinum, phosphorus, hepar sulphuris calcareum, progesterone, oxytocin. This pharmaceutical product is labeled by Carolinas Weight Loss Institute 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: 83014-0008-1. 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: 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 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.

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".