NDC 43857-0487 Additox
Trifolium Pratense,Xanthoxylum Fraxineum,Phytolacca Decandra,Arsenicum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43857-0487?
What are the uses for Additox?
What are Additox Active Ingredients?
- ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- ASPARTAME 30 [hp_X]/mL - Flavoring agent sweeter than sugar, metabolized as PHENYLALANINE and ASPARTIC ACID.
- ATROPA BELLADONNA 12 [hp_X]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BENZALKONIUM CHLORIDE 30 [hp_X]/mL
- CHELIDONIUM MAJUS 12 [hp_X]/mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- FORMALDEHYDE 30 [hp_X]/mL - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- METHYLENE CHLORIDE 30 [hp_X]/mL - A chlorinated hydrocarbon that has been used as an inhalation anesthetic and acts as a narcotic in high concentrations. Its primary use is as a solvent in manufacturing and food technology.
- METHYLPARABEN 30 [hp_X]/mL
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- PROPYLPARABEN 30 [hp_X]/mL
- SODIUM BENZOATE 30 [hp_X]/mL - The sodium salt of BENZOIC ACID. It is used as an antifungal preservative in pharmaceutical preparations and foods. It may also be used as a test for liver function.
- SODIUM CITRATE 30 [hp_X]/mL - Sodium salts of citric acid that are used as buffers and food preservatives. They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.
- TITANIUM DIOXIDE 30 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
- ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
- ZINC OXIDE 30 [hp_X]/mL - A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.
Which are Additox UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T)
- ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- ASPARTAME (UNII: Z0H242BBR1)
- ASPARTAME (UNII: Z0H242BBR1) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- FORMALDEHYDE (UNII: 1HG84L3525)
- FORMALDEHYDE (UNII: 1HG84L3525) (Active Moiety)
- METHYLENE CHLORIDE (UNII: 588X2YUY0A)
- METHYLENE CHLORIDE (UNII: 588X2YUY0A) (Active Moiety)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- METHYLPARABEN (UNII: A2I8C7HI9T) (Active Moiety)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLPARABEN (UNII: Z8IX2SC1OH) (Active Moiety)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Additox 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 Additox?
- Acidifying Activity - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
* 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".