NDC 62795-9491 Lymphomyosot
Araneus Diadematus,Tribasic Calcium Phosphate, Equisetum Hyemale Whole,Ferrous Iodide, - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 62795-9491?
What are the uses for Lymphomyosot?
What are Lymphomyosot Active Ingredients?
- ARANEUS DIADEMATUS 6 [hp_X]/1
- EQUISETUM HYEMALE WHOLE 4 [hp_X]/1
- FERROUS IODIDE 12 [hp_X]/1
- FUMARIA OFFICINALIS FLOWERING TOP 4 [hp_X]/1
- GENTIANA LUTEA ROOT 5 [hp_X]/1
- GERANIUM ROBERTIANUM 4 [hp_X]/1
- JUGLANS REGIA LEAF 3 [hp_X]/1
- LEVOTHYROXINE SODIUM ANHYDROUS 12 [hp_X]/1
- MYOSOTIS ARVENSIS WHOLE 3 [hp_X]/1
- NASTURTIUM OFFICINALE 4 [hp_X]/1 - A plant genus of the family BRASSICACEAE. Nasturtium is also used as a common name for TROPAEOLUM. The common name of watercress is also used for RORIPPA & TROPAEOLUM. This is the most popular of the edible cresses, is a hardy creeping perennial plant, native to Europe but extensively naturalized elsewhere in moist places.
- PINUS SYLVESTRIS LEAFY TWIG 4 [hp_X]/1
- SCROPHULARIA NODOSA WHOLE 3 [hp_X]/1
- SMILAX ORNATA ROOT 6 [hp_X]/1
- SODIUM SULFATE 4 [hp_X]/1
- TEUCRIUM SCORODONIA FLOWERING TOP 3 [hp_X]/1
- TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/1
- VERONICA OFFICINALIS FLOWERING TOP 3 [hp_X]/1
Which are Lymphomyosot UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25)
- EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
- FERROUS IODIDE (UNII: F5452U54PN)
- FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL)
- GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL) (Active Moiety)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
- LEVOTHYROXINE SODIUM ANHYDROUS (UNII: 054I36CPMN)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
- MYOSOTIS ARVENSIS WHOLE (UNII: C73BK97H5J)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
- PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
- VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J)
- VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (Active Moiety)
Which are Lymphomyosot 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:
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
Which are the Pharmacologic Classes for Lymphomyosot?
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Thyroxine - [CS]
- l-Thyroxine - [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".