NDC 0268-8008 5 Grass Mix
Agrostis Gigantea Pollen,Anthoxanthum Odoratum,Dactylis Glomerata,Phleum Pratense,Poa - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0268 - Alk-abello, Inc.
- 0268-8008 - 5 Grass Mix
Product Packages
NDC Code 0268-8008-10
Package Description: 10.5 mL in 1 VIAL
NDC Code 0268-8008-30
Package Description: 32 mL in 1 VIAL
Product Details
What is NDC 0268-8008?
What are the uses for 5 Grass Mix?
What are 5 Grass Mix Active Ingredients?
- AGROSTIS GIGANTEA POLLEN 10000 [PNU]/mL
- ANTHOXANTHUM ODORATUM 10000 [PNU]/mL
- DACTYLIS GLOMERATA 10000 [PNU]/mL
- PHLEUM PRATENSE 10000 [PNU]/mL
- POA PRATENSIS 10000 [PNU]/mL - A plant genus of the family POACEAE that contains the Poa p Ia allergen and allergen C KBGP.
Which are 5 Grass Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
- DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P)
- DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P) (Active Moiety)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
- AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA)
- AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (Active Moiety)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (Active Moiety)
- CYNODON DACTYLON (UNII: 2Q8MR21NHK)
- CYNODON DACTYLON (UNII: 2Q8MR21NHK) (Active Moiety)
- BROMUS INERMIS POLLEN (UNII: 766QT72BK6)
- BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
- XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
- AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
- AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
- PHLEUM PRATENSE (UNII: 0P46LFE4VC)
- PHLEUM PRATENSE (UNII: 0P46LFE4VC) (Active Moiety)
- DACTYLIS GLOMERATA (UNII: 9182Z61D36)
- DACTYLIS GLOMERATA (UNII: 9182Z61D36) (Active Moiety)
- POA PRATENSIS (UNII: ZO990O27NP)
- POA PRATENSIS (UNII: ZO990O27NP) (Active Moiety)
- ANTHOXANTHUM ODORATUM (UNII: YMW1K70E4Q)
- ANTHOXANTHUM ODORATUM (UNII: YMW1K70E4Q) (Active Moiety)
Which are 5 Grass Mix 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:
- POTASSIUM ALUMINATE (UNII: TGN4M9CD7R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for 5 Grass Mix?
- RxCUI: 1922788 - giant ragweed pollen extract 100 UNT/ML / short ragweed pollen extract 100 UNT/ML Injectable Solution
- RxCUI: 1922788 - Ambrosia artemisiifolia pollen extract 100 PNU/ML / Ambrosia trifida pollen extract 100 PNU/ML Injectable Solution
- RxCUI: 1922788 - Ambrosia artemisiifolia pollen extract 100 UNT/ML / Ambrosia trifida pollen extract 100 UNT/ML Injectable Solution
- RxCUI: 1922790 - giant ragweed pollen extract 20000 UNT/ML / short ragweed pollen extract 20000 UNT/ML Injectable Solution
- RxCUI: 1922790 - Ambrosia artemisiifolia pollen extract 20000 PNU/ML / Ambrosia trifida pollen extract 20000 PNU/ML Injectable Solution
Which are the Pharmacologic Classes for 5 Grass Mix?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Pollen Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Pollen - [CS]
- Standardized Pollen 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.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[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".