NDC 43742-1260 Bio Thalamus Phase
Adenosinum Cyclophosphoricum,Apiolum,Melatonin,Pineal Gland (suis),Thalamus Opticus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1260 - Bio Thalamus Phase
Product Packages
NDC Code 43742-1260-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1260?
What are the uses for Bio Thalamus Phase?
What are Bio Thalamus Phase Active Ingredients?
- ADENOSINE CYCLIC PHOSPHATE 6 [hp_X]/mL
- APIOLE (PARSLEY) 6 [hp_X]/mL
- LEVODOPA 8 [hp_X]/mL - The naturally occurring form of DIHYDROXYPHENYLALANINE and the immediate precursor of DOPAMINE. Unlike dopamine itself, it can be taken orally and crosses the blood-brain barrier. It is rapidly taken up by dopaminergic neurons and converted to DOPAMINE. It is used for the treatment of PARKINSONIAN DISORDERS and is usually given with agents that inhibit its conversion to dopamine outside of the central nervous system.
- MELATONIN 6 [hp_X]/mL - A biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.
- SUS SCROFA PINEAL GLAND 8 [hp_X]/mL
- SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS 8 [hp_X]/mL
- VISCUM ALBUM FRUITING TOP 10 [hp_X]/mL
Which are Bio Thalamus Phase UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (Active Moiety)
- APIOLE (PARSLEY) (UNII: QQ67504PXO)
- APIOLE (PARSLEY) (UNII: QQ67504PXO) (Active Moiety)
- MELATONIN (UNII: JL5DK93RCL)
- MELATONIN (UNII: JL5DK93RCL) (Active Moiety)
- SUS SCROFA PINEAL GLAND (UNII: 050QZ2EDK7)
- SUS SCROFA PINEAL GLAND (UNII: 050QZ2EDK7) (Active Moiety)
- SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS (UNII: P146I3107T)
- SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS (UNII: P146I3107T) (Active Moiety)
- LEVODOPA (UNII: 46627O600J)
- LEVODOPA (UNII: 46627O600J) (Active Moiety)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
Which are Bio Thalamus Phase 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 Bio Thalamus Phase?
* 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".