43742-0772 NDC - MALE STIMULANT (ARALIA QUINQUEFOLIA, AGNUS CASTUS, ASCORBICUM ACIDUM, CALADIUM SEGUINUM, KALI BROMATUM, STRYCHNINUM PHOSPHORICUM, CANTHARIS, DAMIANA, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, ORCHITINUM (SUIS), PROSTATE (SUIS), CONIUM MACULATUM, DIENCEPHALON (SUIS), HEART (SUIS), FERRUM PHOSPHORICUM, MAGNESIA PHOSPHORICA, SELENIUM METALLICUM, ZINCUM METALLICUM, PINEAL GLAND (SUIS), CORTISONE ACETICUM, MANGANUM PHOSPHORICUM, LYCOPODIUM CLAVATUM, TESTOSTERONE, MORGAN GAERTNER)

Drug Information

Product NDC: 43742-0772

Proprietary Name: Male Stimulant

Non Proprietary Name: Aralia Quinquefolia, Agnus Castus, Ascorbicum Acidum, Caladium Seguinum, Kali Bromatum, Strychninum Phosphoricum, Cantharis, Damiana, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hypophysis Suis, Orchitinum (Suis), Prostate (Suis), Conium Maculatum, Diencephalon (Suis), Heart (Suis), Ferrum Phosphoricum, Magnesia Phosphorica, Selenium Metallicum, Zincum Metallicum, Pineal Gland (Suis), Cortisone Aceticum, Manganum Phosphoricum, Lycopodium Clavatum, Testosterone, Morgan Gaertner

Active Ingredient(s):
  • 4 [hp_X]/mL AMERICAN GINSENG;
  • 6 [hp_X]/mL ASCORBIC ACID;
  • 6 [hp_X]/mL CHASTE TREE;
  • 8 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP;
  • 13 [hp_X]/mL CORTISONE ACETATE;
  • 6 [hp_X]/mL DIEFFENBACHIA SEGUINE;
  • 10 [hp_X]/mL FERROSOFERRIC PHOSPHATE;
  • 28 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 8 [hp_X]/mL LYTTA VESICATORIA;
  • 10 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 20 [hp_X]/mL MANGANESE PHOSPHATE, DIBASIC;
  • 8 [hp_X]/mL PORK HEART;
  • 6 [hp_X]/mL POTASSIUM BROMIDE;
  • 30 [hp_C]/mL SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS;
  • 10 [hp_X]/mL SELENIUM;
  • 6 [hp_X]/mL STRYCHNINE PHOSPHATE DIHYDRATE;
  • 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND;
  • 8 [hp_X]/mL SUS SCROFA DIENCEPHALON;
  • 12 [hp_X]/mL SUS SCROFA PINEAL GLAND;
  • 8 [hp_X]/mL SUS SCROFA PITUITARY GLAND;
  • 8 [hp_X]/mL SUS SCROFA PROSTATE;
  • 8 [hp_X]/mL SUS SCROFA TESTICLE;
  • 8 [hp_X]/mL SUS SCROFA UMBILICAL CORD;
  • 30 [hp_X]/mL TESTOSTERONE;
  • 8 [hp_X]/mL TURNERA DIFFUSA LEAFY TWIG;
  • 10 [hp_X]/mL ZINC


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Androgen Receptor Agonists [MoA];
  • Androgen [EPC];
  • Androstanes [CS];
  • Ascorbic Acid [CS];
  • Calculi Dissolution Agent [EPC];
  • Corticosteroid Hormone Receptor Agonists [MoA];
  • Corticosteroid [EPC];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Magnetic Resonance Contrast Activity [MoA];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Paramagnetic Contrast Agent [EPC];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE];
  • Vitamin C [EPC]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/8/2016
End Marketing Date:7/16/2023

Package Information

No. Package Code Package Description Billing Unit
143742-0772-130 mL in 1 BOTTLE, DROPPER (43742-0772-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-0772The 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 NAMEMale StimulantThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAralia Quinquefolia, Agnus Castus, Ascorbicum Acidum, Caladium Seguinum, Kali Bromatum, Strychninum Phosphoricum, Cantharis, Damiana, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hypophysis Suis, Orchitinum (Suis), Prostate (Suis), Conium Maculatum, Diencephalon (Suis), Heart (Suis), Ferrum Phosphoricum, Magnesia Phosphorica, Selenium Metallicum, Zincum Metallicum, Pineal Gland (Suis), Cortisone Aceticum, Manganum Phosphoricum, Lycopodium Clavatum, Testosterone, Morgan GaertnerThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE6/8/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE7/16/2023This 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 NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMERICAN GINSENG; ASCORBIC ACID; CHASTE TREE; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; DIEFFENBACHIA SEGUINE; FERROSOFERRIC PHOSPHATE; LYCOPODIUM CLAVATUM SPORE; LYTTA VESICATORIA; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE PHOSPHATE, DIBASIC; PORK HEART; POTASSIUM BROMIDE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SELENIUM; STRYCHNINE PHOSPHATE DIHYDRATE; SUS SCROFA ADRENAL GLAND; SUS SCROFA DIENCEPHALON; SUS SCROFA PINEAL GLAND; SUS SCROFA PITUITARY GLAND; SUS SCROFA PROSTATE; SUS SCROFA TESTICLE; SUS SCROFA UMBILICAL CORD; TESTOSTERONE; TURNERA DIFFUSA LEAFY TWIG; ZINCAn 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 STRENGTH4; 6; 6; 8; 13; 6; 10; 28; 8; 10; 20; 8; 6; 30; 10; 6; 8; 8; 12; 8; 8; 8; 8; 30; 8; 10 
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_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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAndrogen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Ascorbic Acid [CS], Calculi Dissolution Agent [EPC], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin C [EPC] 

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This page was last updated on: 2/1/2023