NDC 55714-4518 Libido

Agnus, Aralia Quinquefolia, Baryta Carb., Berber. Vulg., Bryonia, Caladium Seguinum, Cantharis, Causticum, Chelidonium Majus, Cinchona, Conium, Gaultheria Procumbens, Graphites, Kali Carb., Lycopodium, Nux Vom., Onosmodium Virginianum, Phosphorus, Sabal, Selenium, Sepia, Silicea, Staphysag., Hydrastis, Thuja Occ.

NDC Product Code 55714-4518

NDC Code: 55714-4518

Proprietary Name: Libido 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: Agnus, Aralia Quinquefolia, Baryta Carb., Berber. Vulg., Bryonia, Caladium Seguinum, Cantharis, Causticum, Chelidonium Majus, Cinchona, Conium, Gaultheria Procumbens, Graphites, Kali Carb., Lycopodium, Nux Vom., Onosmodium Virginianum, Phosphorus, Sabal, Selenium, Sepia, Silicea, Staphysag., Hydrastis, Thuja Occ. 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

  • 55714 - Newton Laboratories, Inc.
    • 55714-4518 - Libido

NDC 55714-4518-1

Package Description: 29.57 mL in 1 BOTTLE, GLASS

NDC 55714-4518-2

Package Description: 59.14 mL in 1 BOTTLE, GLASS

NDC Product Information

Libido with NDC 55714-4518 is a a human prescription drug product labeled by Newton Laboratories, Inc.. The generic name of Libido is agnus, aralia quinquefolia, baryta carb., berber. vulg., bryonia, caladium seguinum, cantharis, causticum, chelidonium majus, cinchona, conium, gaultheria procumbens, graphites, kali carb., lycopodium, nux vom., onosmodium virginianum, phosphorus, sabal, selenium, sepia, silicea, staphysag., hydrastis, thuja occ.. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, 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.

Product Type: Human Prescription 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.

Libido 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.

  • CHASTE TREE 20 [hp_X]/mL
  • AMERICAN GINSENG 20 [hp_X]/mL
  • BARIUM CARBONATE 20 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 20 [hp_X]/mL
  • BRYONIA ALBA ROOT 20 [hp_X]/mL
  • DIEFFENBACHIA SEGUINE 20 [hp_X]/mL
  • LYTTA VESICATORIA 20 [hp_X]/mL
  • CAUSTICUM 20 [hp_X]/mL
  • CHELIDONIUM MAJUS 20 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 20 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 20 [hp_X]/mL
  • GAULTHERIA PROCUMBENS TOP 20 [hp_X]/mL
  • GRAPHITE 20 [hp_X]/mL
  • POTASSIUM CARBONATE 20 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 20 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 20 [hp_X]/mL
  • ONOSMODIUM VIRGINIANUM ROOT 20 [hp_X]/mL
  • PHOSPHORUS 20 [hp_X]/mL
  • SAW PALMETTO 20 [hp_X]/mL
  • SELENIUM 20 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 20 [hp_X]/mL
  • SILICON DIOXIDE 20 [hp_X]/mL
  • DELPHINIUM STAPHISAGRIA SEED 20 [hp_X]/mL
  • GOLDENSEAL 8 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 8 [hp_X]/mL

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.

  • 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.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]

Product Labeler Information

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

Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
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: 06-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Libido Product Label Images

Libido 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

Indications & Usage Section

Libido   Formulated for symptoms associated with libido imbalance, hormonal changes and erectile dysfunction.

Dosage & Administration Section

Directions:  ORAL USE ONLY - SHAKE WELL.  Adults, take 6 drops orally one to four times daily or as directed by a healthcare professional.

Active Ingredient Section

Agnus 20x, Aralia quinquefolia 20x, Baryta carb. 20x, Berber. vulg. 20x, Bryonia 20x, Caladium seguinum 20x, Cantharis 20x, Causticum 20x, Chelidonium majus 20x, Cinchona 20x, Conium 20x, Gaultheria procumbens 20x, Graphites 20x, Kali carb. 20x, Lycopodium 20x, Nux vom. 20x, Onosmodium virginianum 20x, Phosphorus 20x, Sabal 20x, Selenium 20x, Sepia 20x, Silicea 20x, Staphysag. 20x, Hydrastis 8x, Thuja occ. 8x, Hydrastis 3x, Thuja occ. 3x.

Purpose Section

Formulated for symptoms associated with libido imbalance, hormonal changes and erectile dysfunction.

Inactive Ingredient Section

Inactive Ingredients:  USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.

Questions? Section

Www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning:  Do not use if tamper - evident seal is broken or missing.  Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.  Keep out of reach of children.

Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.

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