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  5. NDC Package Code: 43742-1379-1 Male Stimulant

NDC Package 43742-1379-1 Male Stimulant

Aralia Quinquefolia,Agnus Castus,Ascorbicum Acidum,Caladium Seguinum,Kali - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
43742-1379-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1379
Proprietary Name:
Male Stimulant
Non-Proprietary Name:
Aralia Quinquefolia, Agnus Castus, Ascorbicum Acidum, Caladium Seguinum, Kali Bromatum, Cantharis, Damiana, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hypophysis Suis, Orchitinum (suis), Prostate (suis), Strychninum Phosphoricum, 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
Substance Name:
American 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; Zinc
Usage Information:
Temporary relief of symptoms related to male hormonal problems such as libido difficulties and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. Temporary relief of symptoms related to male hormonal problems such as libido difficulties and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742137901
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, Inc.
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):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • AMERICAN GINSENG 4 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • CHASTE TREE 6 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 8 [hp_X]/mL
  • CORTISONE ACETATE 13 [hp_X]/mL
  • DIEFFENBACHIA SEGUINE 6 [hp_X]/mL
  • FERROSOFERRIC PHOSPHATE 10 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 28 [hp_X]/mL
  • LYTTA VESICATORIA 8 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/mL
  • MANGANESE PHOSPHATE, DIBASIC 20 [hp_X]/mL
  • PORK HEART 8 [hp_X]/mL
  • POTASSIUM BROMIDE 6 [hp_X]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • SELENIUM 10 [hp_X]/mL
  • STRYCHNINE PHOSPHATE DIHYDRATE 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • SUS SCROFA DIENCEPHALON 8 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 12 [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 8 [hp_X]/mL
  • TESTOSTERONE 30 [hp_X]/mL
  • TURNERA DIFFUSA LEAFY TWIG 8 [hp_X]/mL
  • ZINC 10 [hp_X]/mL
    • Pharmacologic Class(es):
  • Androgen Receptor Agonists - [MoA] (Mechanism of Action)
  • Androgen - [EPC] (Established Pharmacologic Class)
  • Androstanes - [CS]
  • Ascorbic Acid - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
    • DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-05-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 43742-1379-1?

    The NDC Packaged Code 43742-1379-1 is assigned to a package of 30 ml in 1 bottle, dropper of Male Stimulant, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-1379 included in the NDC Directory?

    Yes, Male Stimulant with product code 43742-1379 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on September 05, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43742-1379-1?

    The 11-digit format is 43742137901. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-143742-1379-15-4-243742-1379-01