NDC 43857-0514 Cvtox
Cochlearia Armoracia,Echinacea (angustifolia),Lomatium Dissectum,Tabebuia - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0514 - Cvtox
Product Packages
NDC Code 43857-0514-1
Package Description: 30 mL in 1 PACKAGE
Product Details
What is NDC 43857-0514?
What are the uses for Cvtox?
What are Cvtox Active Ingredients?
- ARANEUS DIADEMATUS 12 [hp_X]/mL
- BOS TAURUS ADRENAL GLAND 8 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- GOLDENSEAL 5 [hp_X]/mL
- HEPATITIS B VIRUS 33 [hp_C]/mL - The type species of the genus ORTHOHEPADNAVIRUS which causes human HEPATITIS B and is also apparently a causal agent in human HEPATOCELLULAR CARCINOMA. The Dane particle is an intact hepatitis virion, named after its discoverer. Non-infectious spherical and tubular particles are also seen in the serum.
- HORSERADISH 3 [hp_X]/mL
- HUMAN COXSACKIEVIRUS B1 15 [hp_C]/mL
- HUMAN COXSACKIEVIRUS B4 15 [hp_C]/mL
- HUMAN HERPESVIRUS 3 30 [hp_X]/mL - The type species of VARICELLOVIRUS causing CHICKENPOX (varicella) and HERPES ZOSTER (shingles) in humans.
- HUMAN HERPESVIRUS 4 30 [hp_X]/mL
- HUMAN HERPESVIRUS 5 16 [hp_C]/mL
- HYDROCHLORIC ACID 12 [hp_X]/mL - A strong corrosive acid that is commonly used as a laboratory reagent. It is formed by dissolving hydrogen chloride in water. GASTRIC ACID is the hydrochloric acid component of GASTRIC JUICE.
- IPECAC 12 [hp_X]/mL - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
- LOMATIUM DISSECTUM ROOT 3 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MEASLES VIRUS 30 [hp_X]/mL - The type species of MORBILLIVIRUS and the cause of the highly infectious human disease MEASLES, which affects mostly children.
- NITRIC ACID 12 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- PHOSPHORIC ACID 12 [hp_X]/mL
- POLIOVIRUS 30 [hp_X]/mL - A species of ENTEROVIRUS which is the causal agent of POLIOMYELITIS in humans. Three serotypes (strains) exist. Transmission is by the fecal-oral route, pharyngeal secretions, or mechanical vector (flies). Vaccines with both inactivated and live attenuated virus have proven effective in immunizing against the infection.
- PROPOLIS WAX 6 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- SUS SCROFA THYMUS 8 [hp_X]/mL
- TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
Which are Cvtox UNII Codes?
The UNII codes for the active ingredients in this product are:
- HORSERADISH (UNII: 8DS6G120HJ)
- HORSERADISH (UNII: 8DS6G120HJ) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N)
- LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N) (Active Moiety)
- TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX)
- HANDROANTHUS IMPETIGINOSUS BARK (UNII: 6GLA1946WX) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYDROCHLORIC ACID (UNII: QTT17582CB) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (Active Moiety)
- HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP)
- HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP) (Active Moiety)
- MEASLES VIRUS (UNII: HT3R7C012Q)
- MEASLES VIRUS (UNII: HT3R7C012Q) (Active Moiety)
- POLIOVIRUS (UNII: FZJ641678T)
- POLIOVIRUS (UNII: FZJ641678T) (Active Moiety)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7) (Active Moiety)
- HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD)
- HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD) (Active Moiety)
- HUMAN COXSACKIEVIRUS B4 (UNII: FYF75V7FDY)
- HUMAN COXSACKIEVIRUS B4 (UNII: FYF75V7FDY) (Active Moiety)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
Which are Cvtox 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 Cvtox?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* 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.
[10] What is the End Marketing Date? - 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.
[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".