NDC 17089-306 Guna-dizzy
.alpha.-ketoglutaric Acid - Ambergris - Anamirta Cocculus Seed - Conium Maculatum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-306 - Guna-dizzy
Product Packages
NDC Code 17089-306-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17089-306?
What are the uses for Guna-dizzy?
What are Guna-dizzy Active Ingredients?
- .ALPHA.-KETOGLUTARIC ACID 6 [hp_X]/30mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
- AMBERGRIS 6 [hp_X]/30mL - A gray substance found in the GASTROINTESTINAL TRACT of the SPERM WHALE.
- ANAMIRTA COCCULUS SEED 4 [hp_X]/30mL
- CONIUM MACULATUM FLOWERING TOP 3 [hp_X]/30mL
- EPINEPHRINE 6 [hp_X]/30mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
- FUMARIC ACID 6 [hp_X]/30mL
- MALIC ACID 6 [hp_X]/30mL
- MELATONIN 4 [hp_C]/30mL - 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.
- MINERAL OIL 8 [hp_X]/30mL - A mixture of liquid hydrocarbons obtained from petroleum. It is used as laxative, lubricant, ointment base, and emollient.
- PTERIDIUM AQUILINUM ROOT 8 [hp_X]/30mL
- PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/30mL - 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).
- QUINHYDRONE 6 [hp_X]/30mL
- QUININE SALICYLATE 6 [hp_X]/30mL
- SUS SCROFA ARTERY 6 [hp_X]/30mL
- SUS SCROFA CEREBELLUM 6 [hp_X]/30mL
- SUS SCROFA PLACENTA 6 [hp_X]/30mL
- THIAMINE HYDROCHLORIDE 4 [hp_X]/30mL
- TOBACCO LEAF 6 [hp_X]/30mL
Which are Guna-dizzy UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- AMBERGRIS (UNII: XTC0D02P6C)
- AMBERGRIS (UNII: XTC0D02P6C) (Active Moiety)
- SUS SCROFA ARTERY (UNII: 63O327782Q)
- SUS SCROFA ARTERY (UNII: 63O327782Q) (Active Moiety)
- SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ)
- SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (Active Moiety)
- QUININE SALICYLATE (UNII: 6DY04L71DR)
- QUININE SALICYLATE (UNII: 6DY04L71DR) (Active Moiety)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- MALIC ACID (UNII: 817L1N4CKP)
- MALIC ACID (UNII: 817L1N4CKP) (Active Moiety)
- MELATONIN (UNII: JL5DK93RCL)
- MELATONIN (UNII: JL5DK93RCL) (Active Moiety)
- MINERAL OIL (UNII: T5L8T28FGP)
- MINERAL OIL (UNII: T5L8T28FGP) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- PTERIDIUM AQUILINUM ROOT (UNII: HQJ5Z3SOIV)
- PTERIDIUM AQUILINUM ROOT (UNII: HQJ5Z3SOIV) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- QUINHYDRONE (UNII: P4A66LQ3QJ)
- QUINHYDRONE (UNII: P4A66LQ3QJ) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- THIAMINE HYDROCHLORIDE (UNII: M572600E5P)
- THIAMINE (UNII: X66NSO3N35) (Active Moiety)
Which are Guna-dizzy 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)
Which are the Pharmacologic Classes for Guna-dizzy?
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Analogs/Derivatives - [Chemical/Ingredient]
- Antimalarial - [EPC] (Established Pharmacologic Class)
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Depigmenting Activity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Melanin Synthesis Inhibitor - [EPC] (Established Pharmacologic Class)
- Melanin Synthesis Inhibitors - [MoA] (Mechanism of Action)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Vitamin B 6 - [Chemical/Ingredient]
- Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [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".