NDC 43857-0523 Androtox
Echinacea (angustifolia),Hydrocotyle Asiatica,Sabal Serrulata,Tabebuia Impetiginosa,Thuja - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0523 - Androtox
Product Packages
NDC Code 43857-0523-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0523?
What are the uses for Androtox?
What are Androtox Active Ingredients?
- ASTRAGALUS PROPINQUUS ROOT 6 [hp_X]/mL
- BOTULINUM TOXIN TYPE A 30 [hp_X]/mL
- CALCIUM SULFATE ANHYDROUS 30 [hp_X]/mL
- CENTELLA ASIATICA WHOLE 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- ESCHERICHIA COLI 30 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
- JUNIPERUS VIRGINIANA TWIG 8 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- PROTEUS MORGANII 30 [hp_X]/mL
- PROTEUS VULGARIS 30 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
- PSEUDOMONAS AERUGINOSA 30 [hp_X]/mL - A species of gram-negative, aerobic, rod-shaped bacteria commonly isolated from clinical specimens (wound, burn, and urinary tract infections). It is also found widely distributed in soil and water. P. aeruginosa is a major agent of nosocomial infection.
- PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL
- RHODODENDRON AUREUM LEAF 12 [hp_X]/mL
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI 33 [hp_X]/mL
- SAW PALMETTO 3 [hp_X]/mL
- SODIUM SULFATE 12 [hp_X]/mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 12 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL
- SUS SCROFA LYMPH 6 [hp_X]/mL
- SUS SCROFA PROSTATE 12 [hp_X]/mL
- SUS SCROFA TESTICLE 12 [hp_X]/mL
- TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 3 [hp_X]/mL
- ZINC GLUCONATE 6 [hp_X]/mL
Which are Androtox UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX)
- HANDROANTHUS IMPETIGINOSUS BARK (UNII: 6GLA1946WX) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- JUNIPERUS VIRGINIANA TWIG (UNII: 532BCG080L)
- JUNIPERUS VIRGINIANA TWIG (UNII: 532BCG080L) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- SUS SCROFA TESTICLE (UNII: KM02613O28)
- SUS SCROFA TESTICLE (UNII: KM02613O28) (Active Moiety)
- SUS SCROFA PROSTATE (UNII: O6UD3347K2)
- SUS SCROFA PROSTATE (UNII: O6UD3347K2) (Active Moiety)
- ANEMONE PRATENSIS (UNII: 8E272251DI)
- ANEMONE PRATENSIS (UNII: 8E272251DI) (Active Moiety)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694)
- BOTULINUM TOXIN TYPE A (UNII: E211KPY694) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- PROTEUS VULGARIS (UNII: 11T9HCO30O)
- PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
- PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N)
- PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N) (Active Moiety)
- PROTEUS MORGANII (UNII: 56X6LID5ZY)
- PROTEUS MORGANII (UNII: 56X6LID5ZY) (Active Moiety)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
Which are Androtox 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Androtox?
- Acetylcholine Release Inhibitor - [EPC] (Established Pharmacologic Class)
- Acetylcholine Release Inhibitors - [MoA] (Mechanism of Action)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Neuromuscular Blockade - [PE] (Physiologic Effect)
- Neuromuscular Blocker - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
* 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.
[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".