NDC 0268-0128 Center-al - Olea Europaea Pollen
Olea Europaea Pollen Injection, Suspension Subcutaneous - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 0268-0128?
What are the uses for Center-al - Olea Europaea Pollen?
What are Center-al - Olea Europaea Pollen Active Ingredients?
Which are Center-al - Olea Europaea Pollen UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
- ACER SACCHARUM POLLEN (UNII: V38QUQ7861)
- ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (Active Moiety)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
- PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR)
- PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (Active Moiety)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
- MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52)
- MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (Active Moiety)
- QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7)
- QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (Active Moiety)
- QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO)
- QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (Active Moiety)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (Active Moiety)
- AVENA SATIVA POLLEN (UNII: A7IKY24TR7)
- AVENA SATIVA POLLEN (UNII: A7IKY24TR7) (Active Moiety)
- OLEA EUROPAEA POLLEN (UNII: 43R41XZ627)
- OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (Active Moiety)
Which are Center-al - Olea Europaea Pollen 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 ALUM (UNII: 1L24V9R23S)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Center-al - Olea Europaea Pollen?
- RxCUI: 1095375 - coast live oak pollen extract 10000 UNT/ML Injectable Suspension
- RxCUI: 1095375 - coast live oak pollen extract 10,000 UNT/ML Injectable Suspension
- RxCUI: 1095407 - mesquite pollen extract 10000 UNT/ML Injectable Suspension
- RxCUI: 1095407 - mesquite pollen extract 10,000 UNT/ML Injectable Suspension
- RxCUI: 2560506 - hard maple pollen extract 10000 UNT/mL Injectable Suspension
Which are the Pharmacologic Classes for Center-al - Olea Europaea Pollen?
* 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".