Vital Male Sexual Energy

Arnica Montana, Avena Sativa, Caladium Seguinum, Carduus Marianus, Damiana, Galium Aparine, Glandula Suprarenalis Suis, Hepar Suis, Hypophysis Suis, Lycopodium Clavatum, Nuphar Luteum, Orchitinum, Panax Ginseng, Phosphoricum Acidum, Populus Tremuloides, Testosterone, Thuja Occidentalis, Thymus Suis, Thyroidinum Suis

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0260

Vital Male Sexual Energy also known as Arnica Montana, Avena Sativa, Caladium Seguinum, Carduus Marianus, Damiana, Galium Aparine, Glandula Suprarenalis Suis, Hepar Suis, Hypophysis Suis, Lycopodium Clavatum, Nuphar Luteum, Orchitinum, Panax Ginseng, Phosphoricum Acidum, Populus Tremuloides, Testosterone, Thuja Occidentalis, Thymus Suis, Thyroidinum Suis is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Vital Male Sexual Energy is 50845-0260. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Vital Male Sexual Energy drug includes Arnica Montana - 3 [hp_X]/mL Asian Ginseng - 1 [hp_X]/mL Avena Sativa Flowering Top - 3 [hp_X]/mL Dieffenbachia Seguine - 6 [hp_X]/mL Galium Aparine - 3 [hp_X]/mL Lycopodium Clavatum Spore - 6 [hp_X]/mL Milk Thistle - 3 [hp_X]/mL Nuphar Luteum Root - 2 [hp_X]/mL Phosphoric Acid - 200 [hp_C]/mL Populus Tremuloides Bark - 1 [hp_X]/mL and more. The currest status of Vital Male Sexual Energy drug is Active.

Drug Information:

Drug NDC:	50845-0260
The 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.
Proprietary Name:	Vital Male Sexual Energy
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Arnica Montana, Avena Sativa, Caladium Seguinum, Carduus Marianus, Damiana, Galium Aparine, Glandula Suprarenalis Suis, Hepar Suis, Hypophysis Suis, Lycopodium Clavatum, Nuphar Luteum, Orchitinum, Panax Ginseng, Phosphoricum Acidum, Populus Tremuloides, Testosterone, Thuja Occidentalis, Thymus Suis, Thyroidinum Suis
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Liddell Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ARNICA MONTANA - 3 [hp_X]/mL ASIAN GINSENG - 1 [hp_X]/mL AVENA SATIVA FLOWERING TOP - 3 [hp_X]/mL DIEFFENBACHIA SEGUINE - 6 [hp_X]/mL GALIUM APARINE - 3 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 6 [hp_X]/mL MILK THISTLE - 3 [hp_X]/mL NUPHAR LUTEUM ROOT - 2 [hp_X]/mL PHOSPHORIC ACID - 200 [hp_C]/mL POPULUS TREMULOIDES BARK - 1 [hp_X]/mL Load more... POPULUS TREMULOIDES LEAF - 1 [hp_X]/mL PORK LIVER - 6 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 12 [hp_X]/mL SUS SCROFA PITUITARY GLAND - 12 [hp_X]/mL SUS SCROFA TESTICLE - 6 [hp_X]/mL SUS SCROFA THYMUS - 6 [hp_X]/mL TESTOSTERONE - 30 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG - 200 [hp_C]/mL THYROID, PORCINE - 12 [hp_X]/mL TURNERA DIFFUSA LEAFY TWIG - 1 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	25 Mar, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	05 May, 2026
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Liddell Laboratories, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000175824 N0000000146 M0001109
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	O80TY208ZW CUQ3A77YXI MA9CQJ3F7F 01800C6E6B Z4B6561488 C88X29Y479 U946SH95EE 714LIU3V6D E4GA8884NN 5543O0CEID Load more... 7IIH57D9E0 6EC706HI7F 398IYQ16YV L0PFEMQ1DT KM02613O28 7B69B0BD62 3XMK78S47O 1NT28V9397 6RV024OAUQ RQ2CFA7WWJ
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class MOA:	Androgen Receptor Agonists [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class EPC:	Androgen [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:	Androstanes [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Androgen Receptor Agonists [MoA] Androgen [EPC] Androstanes [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
DEA Schedule:	CIII
This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
50845-0260-2	1 BOTTLE, SPRAY in 1 CARTON (50845-0260-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0260-1)	25 Mar, 2020	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Vital Male Sexual Energy

Arnica Montana & more..

Liquid
Liddell Laboratories, Inc.
NDC: 50845-0260

Purpose:

Uses: may temporarily relieve symptoms of occasional low male sexual energy, which may include: â¢ decrease in sexual desire â¢ decrease in performance and enjoyment â¢ feeling of fatigue** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Vital male sexual energy arnica montana, avena sativa, caladium seguinum, carduus marianus, damiana, galium aparine, glandula suprarenalis suis, hepar suis, hypophysis suis, lycopodium clavatum, nuphar luteum, orchitinum, panax ginseng, phosphoricum acidum, populus tremuloides, testosterone, thuja occidentalis, thymus suis, thyroidinum suis arnica montana arnica montana avena sativa flowering top avena sativa flowering top dieffenbachia seguine dieffenbachia seguine milk thistle milk thistle turnera diffusa leafy twig turnera diffusa leafy twig galium aparine galium aparine sus scrofa adrenal gland sus scrofa adrenal gland pork liver pork liver sus scrofa pituitary gland sus scrofa pituitary gland lycopodium clavatum spore lycopodium clavatum spore nuphar luteum root nuphar lutea root sus scrofa testicle sus scrofa testicle asian ginseng asian ginseng phosphoric acid phosphoric acid populus tremuloides bark populus tremuloides bark populus tremuloides leaf populus tremuloides leaf testosterone testosterone thuja occidentalis leafy twig thuja occidentalis leafy twig sus scrofa thymus sus scrofa thymus thyroid, porcine sus scrofa thyroid water alcohol

Indications and Usage:

Indications: may temporarily relieve symptoms of occasional low male sexual energy, which may include: â¢ decrease in sexual desire â¢ decrease in performance and enjoyment â¢ feeling of fatigue** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: do not use if you have ever had an allergic reaction to this product or any of its ingredients. stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. if pregnant or breast feeding, ask a doctor before using product. do not use if tamper evident seal around neck of bottle is missing or broken. other information: store at room temperature. warning: cancer - www.p65warnings.ca.gov.

Dosage and Administration:

Directions: adults only: spray twice under the tongue three times a day.

Package Label Principal Display Panel:

Package label display: doctor formulated vitÃl male sexual energy may help restore sexual function such as increasing libido, improving performance, enhancing enjoyment and reducing feelings of fatigue. readily absorbed. safe. no known side effects. easy to use. homeopathic fast acting oral spray liddell 1.0 fl oz (30 ml) vital male sexual energy lbl vital male sexual energy ctn

Further Questions:

Questions: dist. by liddell laboratories, inc. 201 apple blvd. woodbine, ia 51579 www.lidddell.net 1-800-460-7733

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.