NDC 58264-0294 A-2
Soybean,Lima Bean,Kidney Bean,String Bean,Black-eyed Pea,And Pea Solution Sublingual - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0294 - A-2
Product Packages
NDC Code 58264-0294-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0294?
What are the uses for A-2?
What are A-2 Active Ingredients?
- BLACK-EYED PEA 30 [hp_X]/mL
- KIDNEY BEAN 30 [hp_X]/mL
- LIMA BEAN 30 [hp_X]/mL
- PEA 30 [hp_X]/mL - A variable annual leguminous vine that is cultivated for its rounded smooth or wrinkled edible protein-rich seeds, the seed of the pea, and the immature pods with their included seeds. (From Webster's New Collegiate Dictionary, 1973)
- SOYBEAN 30 [hp_X]/mL - An annual legume. The SEEDS of this plant are edible and used to produce a variety of SOY FOODS.
- STRING BEAN 30 [hp_X]/mL
Which are A-2 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOYBEAN (UNII: L7HT8F1ZOD)
- SOYBEAN (UNII: L7HT8F1ZOD) (Active Moiety)
- LIMA BEAN (UNII: 112YH1ZMX2)
- LIMA BEAN (UNII: 112YH1ZMX2) (Active Moiety)
- KIDNEY BEAN (UNII: M98C8416QO)
- KIDNEY BEAN (UNII: M98C8416QO) (Active Moiety)
- STRING BEAN (UNII: N9D69B2Q7Y)
- STRING BEAN (UNII: N9D69B2Q7Y) (Active Moiety)
- BLACK-EYED PEA (UNII: 786YV7B602)
- BLACK-EYED PEA (UNII: 786YV7B602) (Active Moiety)
- PEA (UNII: W4X7H8GYFM)
- PEA (UNII: W4X7H8GYFM) (Active Moiety)
Which are A-2 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-2?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Vegetable Proteins - [CS]
* 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".