NDC 83027-0042 Animal Mix
Glandula Suprarenalis (bovine),Hepar Suis,Histaminum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83027 - Nutritional Specialties, Inc.
- 83027-0042 - Animal Mix
Product Packages
NDC Code 83027-0042-1
Package Description: 60 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 83027-0042?
What are the uses for Animal Mix?
What are Animal Mix Active Ingredients?
- ANAS PLATYRHYNCHOS FEATHER 18 [hp_C]/mL
- ANSER ANSER FEATHER 18 [hp_C]/mL
- BOS TAURUS ADRENAL GLAND 6 [hp_X]/mL
- BOS TAURUS HAIR 15 [hp_C]/mL
- CANIS LUPUS FAMILIARIS HAIR 15 [hp_C]/mL
- CAVIA PORCELLUS HAIR 15 [hp_C]/mL
- CORTICOTROPIN 15 [hp_C]/mL
- EQUUS CABALLUS DANDER 15 [hp_C]/mL
- FELIS CATUS HAIR 15 [hp_C]/mL
- GALLUS GALLUS FEATHER 15 [hp_C]/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.
- ORYCTOLAGUS CUNICULUS HAIR 40 [hp_C]/mL
- PORK LIVER 6 [hp_X]/mL
- RATTUS NORVEGICUS HAIR 15 [hp_C]/mL
- SERINUS CANARIA FEATHER 15 [hp_C]/mL
- SUS SCROFA HAIR 15 [hp_C]/mL
Which are Animal 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)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- SERINUS CANARIA FEATHER (UNII: 9EL3384IQY)
- SERINUS CANARIA FEATHER (UNII: 9EL3384IQY) (Active Moiety)
- FELIS CATUS HAIR (UNII: 1564HD0N96)
- FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- BOS TAURUS HAIR (UNII: TOQ97Z8644)
- BOS TAURUS HAIR (UNII: TOQ97Z8644) (Active Moiety)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
- CAVIA PORCELLUS HAIR (UNII: KBA5Y6X57N)
- CAVIA PORCELLUS HAIR (UNII: KBA5Y6X57N) (Active Moiety)
- EQUUS CABALLUS DANDER (UNII: J81SZ18495)
- EQUUS CABALLUS DANDER (UNII: J81SZ18495) (Active Moiety)
- SUS SCROFA HAIR (UNII: 7Q7T9Z7QUW)
- SUS SCROFA HAIR (UNII: 7Q7T9Z7QUW) (Active Moiety)
- RATTUS NORVEGICUS HAIR (UNII: 69KDL2830A)
- RATTUS NORVEGICUS HAIR (UNII: 69KDL2830A) (Active Moiety)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
- ANSER ANSER FEATHER (UNII: 15XI414745)
- ORYCTOLAGUS CUNICULUS HAIR (UNII: 09N62XQ70Y)
- ORYCTOLAGUS CUNICULUS HAIR (UNII: 09N62XQ70Y) (Active Moiety)
Which are Animal 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 Animal Mix?
- Adrenocorticotropic Hormone - [CS]
- Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
- Allergens - [CS]
- Animal Fur - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Cells, Epidermal - [EXT]
- Dander - [CS]
- Feathers - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Animal Dander Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Animal Hair Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Feather Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Salivary Proteins and Peptides - [CS]
- Standardized Animal Hair 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".