NDC 58264-0329 A-24
Agrostis Gigantea Pollen,Festuca Pratensis Pollen,Poa Pratensis Pollen,Dactylis Glomerata - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0329 - A-24
Product Packages
NDC Code 58264-0329-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0329?
What are the uses for A-24?
What are A-24 Active Ingredients?
- AGROSTIS GIGANTEA POLLEN 30 [hp_X]/mL
- AMARANTHUS RETROFLEXUS POLLEN 30 [hp_X]/mL
- AMBROSIA ACANTHICARPA POLLEN 30 [hp_X]/mL
- AMBROSIA ARTEMISIIFOLIA POLLEN 30 [hp_X]/mL
- AMBROSIA PSILOSTACHYA POLLEN 30 [hp_X]/mL
- AMBROSIA TRIFIDA POLLEN 30 [hp_X]/mL
- ANTHOXANTHUM ODORATUM POLLEN 30 [hp_X]/mL
- CHENOPODIUM ALBUM POLLEN 30 [hp_X]/mL
- CYNODON DACTYLON POLLEN 30 [hp_X]/mL
- DACTYLIS GLOMERATA POLLEN 30 [hp_X]/mL
- FESTUCA PRATENSIS POLLEN 30 [hp_X]/mL
- LOLIUM PERENNE POLLEN 30 [hp_X]/mL
- MEDICAGO SATIVA POLLEN 30 [hp_X]/mL
- PHLEUM PRATENSE POLLEN 30 [hp_X]/mL
- POA PRATENSIS POLLEN 30 [hp_X]/mL
- SOLIDAGO CANADENSIS POLLEN 30 [hp_X]/mL
- SORGHUM HALEPENSE POLLEN 30 [hp_X]/mL
- TRIFOLIUM PRATENSE POLLEN 30 [hp_X]/mL
- XANTHIUM STRUMARIUM POLLEN 30 [hp_X]/mL
Which are the Pharmacologic Classes for A-24?
- Allergens - [CS]
- 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.
[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".