Vital Female Sexual Energy

Agnus Castus, Arnica Montana, Caulophyllum Thalictroides, Cinchona Officinalis, Damiana, Hypophysis Suis, L-arginine, Lactuca Virosa, Onosmodium Virginianum, Oophorinum Suis, Phosphoricum Acidum, Sepia, Thuja Occidentalis

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0035

Vital Female Sexual Energy also known as Agnus Castus, Arnica Montana, Caulophyllum Thalictroides, Cinchona Officinalis, Damiana, Hypophysis Suis, L-arginine, Lactuca Virosa, Onosmodium Virginianum, Oophorinum Suis, Phosphoricum Acidum, Sepia, Thuja Occidentalis is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Vital Female Sexual Energy is 50845-0035. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Vital Female Sexual Energy drug includes Arginine - 6 [hp_X]/mL Arnica Montana - 3 [hp_X]/mL Caulophyllum Thalictroides Root - 6 [hp_X]/mL Chaste Tree - 3 [hp_X]/mL Cinchona Officinalis Bark - 3 [hp_X]/mL Lactuca Virosa - 3 [hp_X]/mL Onosmodium Virginianum Whole - 30 [hp_C]/mL Phosphoric Acid - 200 [hp_C]/mL Sepia Officinalis Juice - 30 [hp_C]/mL Sus Scrofa Ovary - 30 [hp_C]/mL and more. The currest status of Vital Female Sexual Energy drug is Active.

Drug Information:

Drug NDC:	50845-0035
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 Female 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:	Agnus Castus, Arnica Montana, Caulophyllum Thalictroides, Cinchona Officinalis, Damiana, Hypophysis Suis, L-arginine, Lactuca Virosa, Onosmodium Virginianum, Oophorinum Suis, Phosphoricum Acidum, Sepia, Thuja Occidentalis
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:	Spray
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:	ARGININE - 6 [hp_X]/mL ARNICA MONTANA - 3 [hp_X]/mL CAULOPHYLLUM THALICTROIDES ROOT - 6 [hp_X]/mL CHASTE TREE - 3 [hp_X]/mL CINCHONA OFFICINALIS BARK - 3 [hp_X]/mL LACTUCA VIROSA - 3 [hp_X]/mL ONOSMODIUM VIRGINIANUM WHOLE - 30 [hp_C]/mL PHOSPHORIC ACID - 200 [hp_C]/mL SEPIA OFFICINALIS JUICE - 30 [hp_C]/mL SUS SCROFA OVARY - 30 [hp_C]/mL Load more... SUS SCROFA PITUITARY GLAND - 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG - 30 [hp_C]/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:	10 Aug, 2010
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	20 Jun, 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.
UNII:	94ZLA3W45F O80TY208ZW JTJ6HH6YEH 433OSF3U8A S003A158SB 6D74QW4H67 604NK4250S E4GA8884NN QDL83WN8C2 S7YTV04R8O Load more... L0PFEMQ1DT 1NT28V9397 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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
50845-0035-2	1 BOTTLE, SPRAY in 1 CARTON (50845-0035-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0035-1)	21 Apr, 2016	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 Female Sexual Energy

Agnus Castus & more..

Spray
Liddell Laboratories, Inc.
NDC: 50845-0035

Purpose:

Uses: may temporarily relieve symptoms of low female sexual energy, which may include: decrease in sexual desire decrease in responsiveness and enjoyment feelings of fatigue** **these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.

Product Elements:

Vital female sexual energy agnus castus, arnica montana, caulophyllum thalictroides, cinchona officinalis, damiana, hypophysis suis, l-arginine, lactuca virosa, onosmodium virginianum, oophorinum suis, phosphoricum acidum, sepia, thuja occidentalis chaste tree chaste tree arnica montana arnica montana caulophyllum thalictroides root caulophyllum thalictroides root cinchona officinalis bark cinchona officinalis bark turnera diffusa leafy twig turnera diffusa leafy twig arginine arginine lactuca virosa lactuca virosa onosmodium virginianum whole onosmodium virginianum whole sus scrofa ovary sus scrofa ovary phosphoric acid phosphoric acid sus scrofa pituitary gland sus scrofa pituitary gland sepia officinalis juice sepia officinalis juice thuja occidentalis leafy twig thuja occidentalis leafy twig water alcohol

Indications and Usage:

Uses: may temporarily relieve symptoms of low female sexual energy, which may include: â¢ decrease in sexual desire â¢ decrease in responsiveness and enjoyment â¢ feelings of fatigue** **these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.

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, 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 health professional before using product. do not use if tamer evident seal around neck of bottle is missing or broken. other information store at room temperature.

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 vital female sexual energy may help restore sexual function such as increasing libido, improving responsiveness, enhancement 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 female sexual energy label vital female sexual energy carton

Further Questions:

Questions: dist. by: liddell laboratories, inc. 201 apple blvd woodbine, ia 51579 www.liddell.net

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.