Male Stimulant Liquid
NDC Package 43742-1379-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Male Stimulant (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) liquids is temporary relief of symptoms related to male hormonal problems such as libido difficulties and fatigue.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1379.

Identification & Billing

NDC Package Code
43742-1379-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-1379
11-Digit Billing Format
43742137901

Clinical Specifications

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 Fruit; Conium Maculatum Flowering Top; Cortisone Acetate; Dieffenbachia Seguine Whole; 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
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
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.
DEA Schedule
Schedule III (CIII) Substances

Regulatory & Marketing

Labeler Name
Deseret Biologicals, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
09-05-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43742-1379-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Male Stimulant, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains american ginseng; ascorbic acid; chaste tree fruit; conium maculatum flowering top; cortisone acetate; dieffenbachia seguine whole; 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 as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Deseret Biologicals, Inc. on September 05, 2018. The current certification is valid through December 31, 2026.

How is this Deseret Biologicals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742137901. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43742-1379-1
11-Digit CMS (5-4-2)
43742-1379-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.