NDC 43853-0035 Testopro
Avena Sativa,Damiana,Hamamelis Virginiana,Korean Ginseng,Populus Tremuloides,Baryta - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43853 - Problen
- 43853-0035 - Testopro
Product Packages
NDC Code 43853-0035-1
Package Description: 30 mL in 1 BOTTLE
Product Details
What is NDC 43853-0035?
What are Testopro Active Ingredients?
- ASIAN GINSENG 1 [hp_X]/30mL
- AVENA SATIVA FLOWERING TOP 1 [hp_X]/30mL
- BARIUM CARBONATE 8 [hp_X]/30mL
- EPIMEDIUM GRANDIFLORUM TOP 6 [hp_X]/30mL
- EURYCOMA LONGIFOLIA WHOLE 6 [hp_X]/30mL
- FENUGREEK SEED 3 [hp_X]/30mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 1 [hp_X]/30mL
- NUPHAR LUTEA ROOT 3 [hp_X]/30mL
- PHOSPHORIC ACID 12 [hp_X]/30mL
- POPULUS TREMULOIDES WHOLE 1 [hp_X]/30mL
- PORK LIVER 6 [hp_X]/30mL
- SAW PALMETTO 6 [hp_X]/30mL
- SELENIUM 12 [hp_X]/30mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
- SUS SCROFA TESTICLE 6 [hp_X]/30mL
- TESTOSTERONE 30 [hp_X]/30mL - A potent androgenic steroid and major product secreted by the LEYDIG CELLS of the TESTIS. Its production is stimulated by LUTEINIZING HORMONE from the PITUITARY GLAND. In turn, testosterone exerts feedback control of the pituitary LH and FSH secretion. Depending on the tissues, testosterone can be further converted to DIHYDROTESTOSTERONE or ESTRADIOL.
- TRIBULUS TERRESTRIS WHOLE 6 [hp_X]/30mL
- TURNERA DIFFUSA LEAFY TWIG 1 [hp_X]/30mL
Which are Testopro UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- POPULUS TREMULOIDES WHOLE (UNII: MUN0TBE4PE)
- POPULUS TREMULOIDES WHOLE (UNII: MUN0TBE4PE) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- NUPHAR LUTEA ROOT (UNII: 714LIU3V6D)
- NUPHAR LUTEA ROOT (UNII: 714LIU3V6D) (Active Moiety)
- SUS SCROFA TESTICLE (UNII: KM02613O28)
- SUS SCROFA TESTICLE (UNII: KM02613O28) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- TESTOSTERONE (UNII: 3XMK78S47O)
- TESTOSTERONE (UNII: 3XMK78S47O) (Active Moiety)
- TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT)
- TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT) (Active Moiety)
- EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89)
- EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89) (Active Moiety)
- EURYCOMA LONGIFOLIA WHOLE (UNII: 8GOM182CI3)
- EURYCOMA LONGIFOLIA WHOLE (UNII: 8GOM182CI3) (Active Moiety)
- FENUGREEK SEED (UNII: 654825W09Z)
- FENUGREEK SEED (UNII: 654825W09Z) (Active Moiety)
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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Testopro?
* Please review the disclaimer below.
[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".