NDC 83027-0041 Tree Mix
Glandula Suprarenalis (bovine),Hepar Suis,Histaminum Hydrochloricum,Alder,American - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0041?
What are the uses for Tree Mix?
What are Tree Mix Active Ingredients?
- ACER SACCHARUM POLLEN 16 [hp_X]/mL
- ALNUS RUBRA POLLEN 16 [hp_X]/mL
- BETULA PENDULA POLLEN 16 [hp_X]/mL
- BOS TAURUS ADRENAL GLAND 6 [hp_X]/mL
- CARYA GLABRA POLLEN 16 [hp_X]/mL
- CORTICOTROPIN 15 [hp_C]/mL
- CORYLUS AVELLANA POLLEN 16 [hp_X]/mL
- FAGUS SYLVATICA POLLEN 16 [hp_X]/mL
- FRAXINUS EXCELSIOR POLLEN 16 [hp_X]/mL
- HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
- JUNIPERUS VIRGINIANA POLLEN 16 [hp_X]/mL
- PLATANUS X ACERIFOLIA POLLEN 16 [hp_X]/mL
- POPULUS ALBA POLLEN 16 [hp_X]/mL
- PORK LIVER 6 [hp_X]/mL
- QUERCUS ROBUR POLLEN 16 [hp_X]/mL
- SALIX X FRAGILIS POLLEN 16 [hp_X]/mL
- SAMBUCUS CANADENSIS FLOWER 16 [hp_X]/mL
- ULMUS GLABRA POLLEN 16 [hp_X]/mL
Which are Tree Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H)
- ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (Active Moiety)
- ULMUS GLABRA POLLEN (UNII: T2K08L297Q)
- ULMUS GLABRA POLLEN (UNII: T2K08L297Q) (Active Moiety)
- FRAXINUS EXCELSIOR POLLEN (UNII: 1824QUA0U3)
- FRAXINUS EXCELSIOR POLLEN (UNII: 1824QUA0U3) (Active Moiety)
- FAGUS SYLVATICA POLLEN (UNII: 63218N1ZBI)
- FAGUS SYLVATICA POLLEN (UNII: 63218N1ZBI) (Active Moiety)
- JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G)
- JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (Active Moiety)
- SAMBUCUS CANADENSIS FLOWER (UNII: C87P971T6W)
- SAMBUCUS CANADENSIS FLOWER (UNII: C87P971T6W) (Active Moiety)
- CORYLUS AVELLANA POLLEN (UNII: CR2J49TL6L)
- CORYLUS AVELLANA POLLEN (UNII: CR2J49TL6L) (Active Moiety)
- CARYA GLABRA POLLEN (UNII: KPO1Z9N98A)
- CARYA GLABRA POLLEN (UNII: KPO1Z9N98A) (Active Moiety)
- ACER SACCHARUM POLLEN (UNII: V38QUQ7861)
- ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (Active Moiety)
- QUERCUS ROBUR POLLEN (UNII: 4PNW66TTHR)
- QUERCUS ROBUR POLLEN (UNII: 4PNW66TTHR) (Active Moiety)
- PLATANUS X ACERIFOLIA POLLEN (UNII: 77X11O684J)
- PLATANUS X ACERIFOLIA POLLEN (UNII: 77X11O684J) (Active Moiety)
- POPULUS ALBA POLLEN (UNII: VU8C8SB23P)
- POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (Active Moiety)
- BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y)
- BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (Active Moiety)
- SALIX X FRAGILIS POLLEN (UNII: UQ7Z2EA3ZI)
- SALIX X FRAGILIS POLLEN (UNII: UQ7Z2EA3ZI) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
Which are Tree Mix 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Tree Mix?
- Adrenocorticotropic Hormone - [CS]
- Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
- 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]
* 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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".