NDC 58264-0300 A-8
Deciduous Tree Mix Solution Sublingual - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0300 - A-8
Product Packages
NDC Code 58264-0300-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0300?
What are the uses for A-8?
What are A-8 Active Ingredients?
- ACER RUBRUM POLLEN 30 [hp_X]/mL
- ACER SACCHARINUM POLLEN 30 [hp_X]/mL
- ACER SACCHARUM POLLEN 30 [hp_X]/mL
- ALNUS RHOMBIFOLIA POLLEN 30 [hp_X]/mL
- ALNUS RUBRA POLLEN 30 [hp_X]/mL
- ALNUS SERRULATA POLLEN 30 [hp_X]/mL
- BETULA LENTA POLLEN 30 [hp_X]/mL
- BETULA NIGRA POLLEN 30 [hp_X]/mL
- BETULA POPULIFOLIA POLLEN 30 [hp_X]/mL
- BROUSSONETIA PAPYRIFERA POLLEN 30 [hp_X]/mL
- CARYA ALBA POLLEN 30 [hp_X]/mL
- CARYA GLABRA POLLEN 30 [hp_X]/mL
- CARYA LACINIOSA POLLEN 30 [hp_X]/mL
- CARYA OVATA POLLEN 30 [hp_X]/mL
- MORUS ALBA POLLEN 30 [hp_X]/mL
- MORUS RUBRA POLLEN 30 [hp_X]/mL
- POPULUS BALSAMIFERA POLLEN 30 [hp_X]/mL
- POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN 30 [hp_X]/mL
- POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN 30 [hp_X]/mL
- ULMUS AMERICANA POLLEN 30 [hp_X]/mL
- ULMUS PUMILA POLLEN 30 [hp_X]/mL
Which are A-8 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H)
- ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (Active Moiety)
- ALNUS SERRULATA POLLEN (UNII: 390VZ1D0L5)
- ALNUS SERRULATA POLLEN (UNII: 390VZ1D0L5) (Active Moiety)
- ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM)
- ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (Active Moiety)
- BETULA LENTA POLLEN (UNII: JQ5HI5004M)
- BETULA LENTA POLLEN (UNII: JQ5HI5004M) (Active Moiety)
- BETULA NIGRA POLLEN (UNII: 93963RFO1P)
- BETULA NIGRA POLLEN (UNII: 93963RFO1P) (Active Moiety)
- BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U)
- BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (Active Moiety)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
- ULMUS PUMILA POLLEN (UNII: 030R993R8E)
- ULMUS PUMILA POLLEN (UNII: 030R993R8E) (Active Moiety)
- POPULUS BALSAMIFERA POLLEN (UNII: A7XVZ7S0Y5)
- POPULUS BALSAMIFERA POLLEN (UNII: A7XVZ7S0Y5) (Active Moiety)
- POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN (UNII: 476DVV63WP)
- POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN (UNII: 476DVV63WP) (Active Moiety)
- POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441)
- POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (Active Moiety)
- CARYA GLABRA POLLEN (UNII: KPO1Z9N98A)
- CARYA GLABRA POLLEN (UNII: KPO1Z9N98A) (Active Moiety)
- CARYA OVATA POLLEN (UNII: 54UN9R2798)
- CARYA OVATA POLLEN (UNII: 54UN9R2798) (Active Moiety)
- CARYA LACINIOSA POLLEN (UNII: 5BGG872373)
- CARYA LACINIOSA POLLEN (UNII: 5BGG872373) (Active Moiety)
- CARYA ALBA POLLEN (UNII: G2A764T54B)
- CARYA ALBA POLLEN (UNII: G2A764T54B) (Active Moiety)
- ACER RUBRUM POLLEN (UNII: 700NK45C76)
- ACER RUBRUM POLLEN (UNII: 700NK45C76) (Active Moiety)
- ACER SACCHARUM POLLEN (UNII: V38QUQ7861)
- ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (Active Moiety)
- ACER SACCHARINUM POLLEN (UNII: 95447163DG)
- ACER SACCHARINUM POLLEN (UNII: 95447163DG) (Active Moiety)
- MORUS ALBA POLLEN (UNII: 3I9T68187H)
- MORUS ALBA POLLEN (UNII: 3I9T68187H) (Active Moiety)
- MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52)
- MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (Active Moiety)
- BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML)
- BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML) (Active Moiety)
Which are A-8 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-8?
* 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".