NDC 43742-1379 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

NDC Product Code 43742-1379

NDC CODE: 43742-1379

Proprietary Name: Male Stimulant What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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 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.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1379-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Male Stimulant with NDC 43742-1379 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Male Stimulant is 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. The product's dosage form is liquid and is administered via oral form.

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.

Product Type: Human Otc Drug 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.

DEA Schedule: Schedule III (CIII) Substances What is the Drug Enforcement Administration (DEA) CIII Schedule?
The controlled substances in the CIII schedule have an abuse potential and dependence liability less than those in schedules CI and CII, and have an accepted medical use in the United States. Schedule CIII controlled substances include preparations containing limited quantities of certain narcotic drugs, and other nonnarcotic drugs such as: derivatives of barbituric acid, except those that are listed in another schedule, glutethimide (Doriden), methyprylon (Noludar), nalorphine, benzphetamine, chlorphentermine, clortermine, and phendimetrazine.

Male Stimulant Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 09-05-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 05-25-2026 What is the End Marketing Date?
This 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.

Exclude Flag: N - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Male Stimulant Product Label Images

Male Stimulant Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Aralia Quinquefolia 4X, Agnus Castus 6X, Ascorbicum Acidum 6X, Caladium Seguinum 6X, Kali Bromatum 6X, Cantharis 8X, Damiana 8X, Funiculus Umbilicalis Suis 8X, Glandula Suprarenalis Suis 8X, Hypophysis Suis 8X, Orchitinum (Suis) 8X, Prostate (Suis) 8X, Strychninum Phosphoricum 8X, Conium Maculatum 8X, 28X, Diencephalon (Suis) 8X, 30X, 200X, Heart (Suis) 8X, 30X, 200X, Ferrum Phosphoricum 10X, Magnesia Phosphorica 10X, Selenium Metallicum 10X, Zincum Metallicum 10X, Pineal Gland (Suis) 12X, 30X, 200X, Cortisone Aceticum 13X, Manganum Phosphoricum 20X, Lycopodium Clavatum 28X, Testosterone 30X, 60X, 200X, Morgan Gaertner 30C, 200C.

Homeopathic Indications:

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.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1379-1HOMEOPATHICMALESTIMULANT1 FL OZ (30 ml)

* Please review the disclaimer below.