NDC 43853-0035 Testopro

Avena Sativa,Damiana,Hamamelis Virginiana,Korean Ginseng,Populus Tremuloides,Baryta - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43853-0035
Proprietary Name:
Testopro
Non-Proprietary Name: [1]
Avena Sativa, Damiana, Hamamelis Virginiana, Korean Ginseng, Populus Tremuloides, Baryta Carbonica, Hepar Suis, Nuphar Luteum, Orchitinum Suis, Phosphoricum Acidum, Sabal Serulata, Selenium Metallicum, Testosterone, Tribulus Terrestris, Horny Goat Weed, Tongkat Ali, Fenugreek
Substance Name: [2]
Asian Ginseng; Avena Sativa Flowering Top; Barium Carbonate; Epimedium Grandiflorum Top; Eurycoma Longifolia Whole; Fenugreek Seed; Hamamelis Virginiana Root Bark/stem Bark; Nuphar Lutea Root; Phosphoric Acid; Populus Tremuloides Whole; Pork Liver; Saw Palmetto; Selenium; Sus Scrofa Testicle; Testosterone; Tribulus Terrestris Whole; Turnera Diffusa Leafy Twig
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Problen
    Labeler Code:
    43853
    DEA Schedule: [7]
    Schedule III (CIII) Substances
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    06-28-2017
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43853-0035-1

    Package Description: 30 mL in 1 BOTTLE

    Product Details

    What is NDC 43853-0035?

    The NDC code 43853-0035 is assigned by the FDA to the product Testopro which is a human over the counter drug product labeled by Problen. The generic name of Testopro is avena sativa, damiana, hamamelis virginiana, korean ginseng, populus tremuloides, baryta carbonica, hepar suis, nuphar luteum, orchitinum suis, phosphoricum acidum, sabal serulata, selenium metallicum, testosterone, tribulus terrestris, horny goat weed, tongkat ali, fenugreek. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 43853-0035-1 30 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are Testopro Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Testopro UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Testopro Inactive Ingredients UNII Codes?

    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. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Testopro?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [7] What is the Drug Enforcement Administration (DEA) CIII Schedule? - This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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".