A-24 Solution
NDC 58264-0329
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
A-24 (agrostis gigantea pollen, festuca pratensis pollen, poa pratensis pollen, dactylis glomerata pollen, phleum pratense pollen, anthoxanthum odoratum pollen, lolium perenne pollen, medicago sativa pollen, trifolium pratense pollen, solidago canadensis pollen, ambrosia acanthicarpa pollen, ambrosia psilostachya pollen, ambrosia trifida pollen, ambrosia artemisiifolia pollen, xanthium strumarium pollen, chenopodium album pollen, amaranthus retroflexus pollen, and cynodon dactylon pollen) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Dna Labs, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a solution for sublingual administration. This product entry covers the primary NDC 58264-0329 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
58264-0329
Proprietary Name:
A-24
Non-Proprietary Name: [1]
Agrostis Gigantea Pollen, Festuca Pratensis Pollen, Poa Pratensis Pollen, Dactylis Glomerata Pollen, Phleum Pratense Pollen, Anthoxanthum Odoratum Pollen, Lolium Perenne Pollen, Medicago Sativa Pollen, Trifolium Pratense Pollen, Solidago Canadensis Pollen, Ambrosia Acanthicarpa Pollen, Ambrosia Psilostachya Pollen, Ambrosia Trifida Pollen, Ambrosia Artemisiifolia Pollen, Xanthium Strumarium Pollen, Chenopodium Album Pollen, Amaranthus Retroflexus Pollen, And Cynodon Dactylon Pollen
Substance Name: [2]
Agrostis Gigantea Pollen; Amaranthus Retroflexus Pollen; Ambrosia Acanthicarpa Pollen; Ambrosia Artemisiifolia Pollen; Ambrosia Psilostachya Pollen; Ambrosia Trifida Pollen; Anthoxanthum Odoratum Pollen; Chenopodium Album Pollen; Cynodon Dactylon Pollen; Dactylis Glomerata Pollen; Festuca Pratensis Pollen; Lolium Perenne Pollen; Medicago Sativa Pollen; Phleum Pratense Pollen; Poa Pratensis Pollen; Solidago Canadensis Pollen; Sorghum Halepense Pollen; Trifolium Pratense Pollen; Xanthium Strumarium Pollen
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Solution
- A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s): [4]
Sublingual - Administration beneath the tongue.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
58264
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
01-01-1990
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 58264-0329?
The NDC code 58264-0329 is assigned by the FDA to the product A-24. It is commonly known by its generic name, agrostis gigantea pollen, festuca pratensis pollen, poa pratensis pollen, dactylis glomerata pollen, phleum pratense pollen, anthoxanthum odoratum pollen, lolium perenne pollen, medicago sativa pollen, trifolium pratense pollen, solidago canadensis pollen, ambrosia acanthicarpa pollen, ambrosia psilostachya pollen, ambrosia trifida pollen, ambrosia artemisiifolia pollen, xanthium strumarium pollen, chenopodium album pollen, amaranthus retroflexus pollen, and cynodon dactylon pollen. This pharmaceutical product is labeled by Dna Labs, Inc. and is currently categorized as listed product. The medication is a solution administered via sublingual route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 58264-0329-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
This product is used as Allergies.
What are Active Ingredients of this product?
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.
- 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 of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
- 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)
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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
