83014-0003 NDC - WEIGHT LOSS SUPPORT PLUS MALE BALANCE (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)

Drug Information

  • Product NDC: 83014-0003
  • Proprietary Name: Weight Loss Support Plus Male Balance
  • Non Proprietary Name: 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
  • Active Ingredient(s): 3 [hp_X]/mL AMMONIUM BROMIDE; 9 [hp_X]/mL ANTIMONY TRISULFIDE; 8 [hp_X]/mL BOS TAURUS PITUITARY GLAND, POSTERIOR; 16 [hp_X]/mL BOS TAURUS TESTICLE; 6 [hp_X]/mL CAPSICUM; 2 [hp_X]/mL CHASTE TREE FRUIT; 3 [hp_X]/mL DIEFFENBACHIA SEGUINE WHOLE; 3 [hp_X]/mL EGG PHOSPHOLIPIDS; 12 [hp_X]/mL EPINEPHRINE; 2 [hp_X]/mL FOENICULUM VULGARE FRUIT; 3 [hp_X]/mL FUCUS VESICULOSUS; 6 [hp_X]/mL GALIUM APARINE WHOLE; 30 [hp_C]/mL ONOSMODIUM VIRGINIANUM; 9 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 12 [hp_X]/mL PHOSPHORUS; 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 6 [hp_X]/mL POTASSIUM DICHROMATE; 9 [hp_X]/mL SELENIUM; 9 [hp_X]/mL SILVER; 6 [hp_X]/mL SKIM MILK; 6 [hp_X]/mL SUS SCROFA PITUITARY GLAND; 6 [hp_X]/mL THYROID, BOVINE
  • Administration Route(s): ORAL
  • Dosage Form(s): SPRAY
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Vegetable Proteins [CS]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Carolinas Weight Loss Institute
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/10/2023
End Marketing Date:6/14/2028

Package Information

No. Package Code Package Description Billing Unit
183014-0003-160 mL in 1 BOTTLE, SPRAY (83014-0003-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83014-0003The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEWeight Loss Support Plus Male BalanceThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAgnus 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 VirginianumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/10/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE6/14/2028This 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.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMECarolinas Weight Loss InstituteName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMMONIUM 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, BOVINEAn 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.
ACTIVE NUMERATOR STRENGTH3; 9; 8; 16; 6; 2; 3; 3; 12; 2; 3; 6; 30; 9; 12; 6; 6; 9; 9; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 3/6/2026

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