NDC 58264-0314 A-22
Aspergillus Flavus,Aspergillus Fumigatus,Eurotium Herbariorum,Aspergillus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0314 - A-22
Product Packages
NDC Code 58264-0314-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0314?
What are the uses for A-22?
What are A-22 Active Ingredients?
- ASPERGILLUS FLAVUS 30 [hp_X]/mL - A species of imperfect fungi which grows on peanuts and other plants and produces the carcinogenic substance aflatoxin. It is also used in the production of the antibiotic flavicin.
- ASPERGILLUS FUMIGATUS 30 [hp_X]/mL - A species of imperfect fungi from which the antibiotic fumigatin is obtained. Its spores may cause respiratory infection in birds and mammals.
- ASPERGILLUS NIDULANS 30 [hp_X]/mL - A species of imperfect fungi from which the antibiotic nidulin is obtained. Its teleomorph is Emericella nidulans.
- ASPERGILLUS NIGER VAR. NIGER 30 [hp_X]/mL
- EUROTIUM HERBARIORUM 30 [hp_X]/mL
- PENICILLIUM CAMEMBERTI 30 [hp_X]/mL
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 30 [hp_X]/mL
- PENICILLIUM DIGITATUM 30 [hp_X]/mL
- PENICILLIUM ROQUEFORTI 30 [hp_X]/mL
Which are A-22 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (Active Moiety)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Active Moiety)
- EUROTIUM HERBARIORUM (UNII: 49W168AES4)
- EUROTIUM HERBARIORUM (UNII: 49W168AES4) (Active Moiety)
- ASPERGILLUS NIDULANS (UNII: 242A53RB80)
- ASPERGILLUS NIDULANS (UNII: 242A53RB80) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG)
- PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (Active Moiety)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (Active Moiety)
- PENICILLIUM DIGITATUM (UNII: 1SB49SV239)
- PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (Active Moiety)
- PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L)
- PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (Active Moiety)
Which are A-22 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 A-22?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Fungal Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Fungal 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".