NDC 64578-0171 Hypothalmapath
Gelsemium,Ginkgo,Glycyrrhiza,Hydrocotyle,Hypothalamus,Petroselinum,Pituitarum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64578 - Energetix Corporation
- 64578-0171 - Hypothalmapath
Product Packages
NDC Code 64578-0171-1
Package Description: 59.1 mL in 1 BOTTLE
Product Details
What is NDC 64578-0171?
What are Hypothalmapath Active Ingredients?
- BOS TAURUS HYPOTHALAMUS 12 [hp_X]/59.1mL
- CENTELLA ASIATICA WHOLE 4 [hp_X]/59.1mL
- GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/59.1mL
- GINKGO 6 [hp_X]/59.1mL
- LICORICE 4 [hp_X]/59.1mL
- PETROSELINUM CRISPUM WHOLE 4 [hp_X]/59.1mL
- PYRIDOXINE HYDROCHLORIDE 12 [hp_X]/59.1mL - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
- SENNA LEAF 8 [hp_X]/59.1mL
- SILICON DIOXIDE 12 [hp_X]/59.1mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- SUS SCROFA PITUITARY GLAND, POSTERIOR 12 [hp_X]/59.1mL
Which are Hypothalmapath UNII Codes?
The UNII codes for the active ingredients in this product are:
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- LICORICE (UNII: 61ZBX54883)
- LICORICE (UNII: 61ZBX54883) (Active Moiety)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)
- PETROSELINUM CRISPUM WHOLE (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Hypothalmapath 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Hypothalmapath?
* 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".