NDC 43857-0640 Apizelen
Germanium Metallicum,Alfalfa,Aralia Quinquefolia,Avena Sativa,Beta Vulgaris,Calendula - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43857-0640?
What are the uses for Apizelen?
What are Apizelen Active Ingredients?
- AMERICAN GINSENG 2 [hp_C]/mL
- AVENA SATIVA FLOWERING TOP 2 [hp_C]/mL
- BETA VULGARIS WHOLE 2 [hp_C]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_C]/mL
- CHELIDONIUM MAJUS WHOLE 2 [hp_C]/mL
- COBALTOUS ACETATE 3 [hp_C]/mL
- COBALTOUS GLUCONATE 3 [hp_C]/mL
- COPPER GLUCONATE 3 [hp_C]/mL - Derivatives of gluconic acid (the structural formula HOCH2(CHOH)4COOH), including its salts and esters.
- CUPRIC ACETATE 3 [hp_C]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 2 [hp_C]/mL
- GERMANIUM 15 [hp_X]/mL - A rare metal element with a blue-gray appearance and atomic symbol Ge, atomic number 32, and atomic weight 72.63.
- GLUTATHIONE 3 [hp_C]/mL - A tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides.
- LARREA TRIDENTATA LEAF 2 [hp_C]/mL
- MAGNESIUM GLUCONATE 3 [hp_C]/mL
- MEDICAGO SATIVA WHOLE 2 [hp_C]/mL
- PHYTOLACCA AMERICANA ROOT 2 [hp_C]/mL
- REISHI 5 [hp_C]/mL - A mushroom, Ganoderma lucidum, of the POLYPORALES order of basidiomycetous fungi. It has long been used in traditional Chinese medicine in various forms.
- SILVER 8 [hp_C]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
- SODIUM CHLORIDE 2 [hp_C]/mL - A ubiquitous sodium salt that is commonly used to season food.
- TARAXACUM OFFICINALE 2 [hp_C]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- TRIFOLIUM PRATENSE FLOWER 2 [hp_C]/mL
- UBIDECARENONE 5 [hp_C]/mL
- URTICA DIOICA WHOLE 2 [hp_C]/mL
- VISCUM ALBUM FRUITING TOP 2 [hp_C]/mL
Which are Apizelen UNII Codes?
The UNII codes for the active ingredients in this product are:
- GERMANIUM (UNII: 00072J7XWS)
- GERMANIUM (UNII: 00072J7XWS) (Active Moiety)
- MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
- AMERICAN GINSENG (UNII: 8W75VCV53Q)
- AMERICAN GINSENG (UNII: 8W75VCV53Q) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- BETA VULGARIS WHOLE (UNII: 4G174V5051)
- BETA VULGARIS (UNII: 4G174V5051) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- URTICA DIOICA WHOLE (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
- COBALTOUS ACETATE (UNII: 3XC4P44U7E)
- COBALTOUS CATION (UNII: AI1MR454XG) (Active Moiety)
- COBALTOUS GLUCONATE (UNII: 26SK597UWV)
- COPPER GLUCONATE (UNII: RV823G6G67)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- CUPRIC ACETATE (UNII: 39M11XPH03)
- GLUTATHIONE (UNII: GAN16C9B8O)
- GLUTATHIONE (UNII: GAN16C9B8O) (Active Moiety)
- MAGNESIUM GLUCONATE (UNII: T42NAD2KHC)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- REISHI (UNII: TKD8LH0X2Z)
- REISHI (UNII: TKD8LH0X2Z) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
Which are Apizelen 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 Apizelen?
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* 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".