NDC 43742-1340 Vertigone
Natrum Salicylicum,Cerebellum (suis),Bryonia (alba),Petroleum,Tabacum,Ambra - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43742-1340?
What are the uses for Vertigone?
What are Vertigone Active Ingredients?
- AMBERGRIS 9 [hp_X]/mL - A gray substance found in the GASTROINTESTINAL TRACT of the SPERM WHALE.
- ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
- ASARUM CANADENSE ROOT 12 [hp_X]/mL
- BRYONIA ALBA ROOT 8 [hp_X]/mL
- CALCIUM SULFATE ANHYDROUS 12 [hp_X]/mL
- CARBON DISULFIDE 12 [hp_X]/mL - A colorless, flammable, poisonous liquid, CS2. It is used as a solvent, and is a counterirritant and has local anesthetic properties but is not used as such. It is highly toxic with pronounced CNS, hematologic, and dermatologic effects.
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- CYCLAMEN PURPURASCENS TUBER 9 [hp_X]/mL
- DIGITALIS 12 [hp_X]/mL - A genus of toxic herbaceous Eurasian plants of the Plantaginaceae which yield cardiotonic DIGITALIS GLYCOSIDES. The most useful species are Digitalis lanata and D. purpurea.
- GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
- KEROSENE 8 [hp_X]/mL - A refined petroleum fraction used as a fuel as well as a solvent.
- MACROPIPER METHYSTICUM ROOT 12 [hp_X]/mL
- PHOSPHORUS 12 [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.
- QUININE SULFATE 12 [hp_X]/mL - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
- 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.
- SILVER NITRATE 12 [hp_X]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
- SODIUM SALICYLATE 3 [hp_X]/mL - A non-steroidal anti-inflammatory agent that is less effective than equal doses of ASPIRIN in relieving pain and reducing fever. However, individuals who are hypersensitive to ASPIRIN may tolerate sodium salicylate. In general, this salicylate produces the same adverse reactions as ASPIRIN, but there is less occult gastrointestinal bleeding. (From AMA Drug Evaluations Annual, 1992, p120)
- SUS SCROFA CEREBELLUM 6 [hp_X]/mL
- THERIDION CURASSAVICUM 12 [hp_X]/mL
- TOBACCO LEAF 8 [hp_X]/mL
Which are Vertigone UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ)
- SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- AMBERGRIS (UNII: XTC0D02P6C)
- AMBERGRIS (UNII: XTC0D02P6C) (Active Moiety)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ASARUM CANADENSE ROOT (UNII: E2O4O7TQYK)
- ASARUM CANADENSE ROOT (UNII: E2O4O7TQYK) (Active Moiety)
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CARBON DISULFIDE (UNII: S54S8B99E8)
- CARBON DISULFIDE (UNII: S54S8B99E8) (Active Moiety)
- QUININE SULFATE (UNII: KF7Z0E0Q2B)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- DIGITALIS (UNII: F1T8QT9U8B)
- DIGITALIS (UNII: F1T8QT9U8B) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- MACROPIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
- MACROPIPER METHYSTICUM ROOT (UNII: BOW48C81XP) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- THERIDION CURASSAVICUM (UNII: 9Z8D3HEM8L)
- THERIDION CURASSAVICUM (UNII: 9Z8D3HEM8L) (Active Moiety)
Which are Vertigone 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 Vertigone?
- Allergens - [CS]
- Antimalarial - [EPC] (Established Pharmacologic Class)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- 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".