NDC 43406-0100 Weed Grass Antigen
Alopecurus Pratensis,Anthoxanthum,Cynodon,Melilotus Off,Phleum Pratense,Rumex Crisp,Secale - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43406-0100?
What are the uses for Weed Grass Antigen?
What are Weed Grass Antigen Active Ingredients?
- ALOPECURUS PRATENSIS 30 [hp_X]/mL
- AMBROSIA ARTEMISIIFOLIA WHOLE 30 [hp_C]/mL
- ANTHOXANTHUM ODORATUM WHOLE 30 [hp_X]/mL
- ARSENIC TRIOXIDE 30 [hp_C]/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 WHOLE 30 [hp_X]/mL
- MELILOTUS OFFICINALIS TOP 30 [hp_X]/mL
- ONION 30 [hp_C]/mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PHLEUM PRATENSE POLLEN 30 [hp_X]/mL
- PULSATILLA VULGARIS WHOLE 30 [hp_C]/mL
- RUMEX CRISPUS ROOT 30 [hp_X]/mL
- SECALE CEREALE WHOLE 30 [hp_X]/mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 30 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/mL
- WHEAT BRAN 30 [hp_X]/mL - The remnants of plant cell walls that are resistant to digestion by the alimentary enzymes of man. It comprises various polysaccharides and lignins.
Which are Weed Grass Antigen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOPECURUS PRATENSIS (UNII: T306U9V415)
- ALOPECURUS PRATENSIS (UNII: T306U9V415) (Active Moiety)
- ANTHOXANTHUM ODORATUM WHOLE (UNII: YMW1K70E4Q)
- ANTHOXANTHUM ODORATUM (UNII: YMW1K70E4Q) (Active Moiety)
- CYNODON DACTYLON WHOLE (UNII: 2Q8MR21NHK)
- CYNODON DACTYLON WHOLE (UNII: 2Q8MR21NHK) (Active Moiety)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX) (Active Moiety)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
- PHLEUM PRATENSE TOP (UNII: S7PW24BX20) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- SECALE CEREALE WHOLE (UNII: 12M71ST1GZ)
- SECALE CEREALE WHOLE (UNII: 12M71ST1GZ) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- WHEAT BRAN (UNII: 6L966A1IMR)
- WHEAT BRAN (UNII: 6L966A1IMR) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (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 VULGARIS WHOLE (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
Which are Weed 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Weed 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)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- 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".