NDC 48951-8396 Reynoutria Lyme
Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy, Inc.
- 48951-8396 - Reynoutria Lyme
Product Packages
NDC Code 48951-8396-3
Package Description: 60 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 48951-8396?
What are the uses for Reynoutria Lyme?
What are Reynoutria Lyme Active Ingredients?
- APIS MELLIFERA 21 [hp_X]/mL
- ASTRAGALUS CHINENSIS SEED 30 [hp_X]/mL
- ASTRAGALUS PROPINQUUS ROOT 6 [hp_X]/mL
- COPPER 17 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- DIPSACUS FULLONUM WHOLE 4 [hp_X]/mL
- GOLD 30 [hp_X]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
- HELLEBORUS NIGER ROOT 4 [hp_X]/mL
- REYNOUTRIA JAPONICA LEAF 3 [hp_X]/mL
- SILICON DIOXIDE 17 [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 17 [hp_X]/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.
Which are Reynoutria Lyme UNII Codes?
The UNII codes for the active ingredients in this product are:
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ASTRAGALUS CHINENSIS SEED (UNII: U046B39ADE)
- ASTRAGALUS CHINENSIS SEED (UNII: U046B39ADE) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
- DIPSACUS FULLONUM WHOLE (UNII: 1FT87R544S)
- DIPSACUS FULLONUM WHOLE (UNII: 1FT87R544S) (Active Moiety)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
- REYNOUTRIA JAPONICA LEAF (UNII: 2540B7G25G)
- REYNOUTRIA JAPONICA LEAF (UNII: 2540B7G25G) (Active Moiety)
Which are Reynoutria Lyme 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 Reynoutria Lyme?
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [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".