NDC 43857-0562 Weed And Grass Antigen
Allium Cepa,Arsenicum Album,Nux Vomica,Pulsatilla Pratensis,Kentucky Bluegrass,Orchard - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43857-0562?
What are the uses for Weed And Grass Antigen?
What are Weed And Grass Antigen Active Ingredients?
- ANTHOXANTHUM ODORATUM POLLEN 12 [hp_X]/mL
- 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.
- CYNODON DACTYLON POLLEN 12 [hp_X]/mL
- DACTYLIS GLOMERATA TOP 12 [hp_X]/mL
- LOLIUM PERENNE POLLEN 12 [hp_X]/mL
- ONION 12 [hp_X]/mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PASPALUM NOTATUM POLLEN 12 [hp_X]/mL
- PHLEUM PRATENSE TOP 12 [hp_X]/mL
- POA PRATENSIS POLLEN 12 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL
- SORGHUM HALEPENSE POLLEN 12 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
Which are Weed And Grass Antigen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI)
- PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (Active Moiety)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
- DACTYLIS GLOMERATA TOP (UNII: J41552QKAK)
- DACTYLIS GLOMERATA TOP (UNII: J41552QKAK) (Active Moiety)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10)
- CYNODON DACTYLON WHOLE (UNII: 2Q8MR21NHK) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0)
- LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0) (Active Moiety)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (Active Moiety)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)
- PHLEUM PRATENSE TOP (UNII: S7PW24BX20)
- PHLEUM PRATENSE TOP (UNII: S7PW24BX20) (Active Moiety)
Which are Weed And Grass Antigen 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 Weed And Grass Antigen?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Pollen Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Pollen - [CS]
- Seed Storage Proteins - [CS]
- Standardized Pollen Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable 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.
[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".