NDC 17089-347 Guna-hypertension
Arnica Montana - Fumaric Acid - Gold - Lead - Melatonin - Melilotus - Olea Europaea Flower - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-347 - Guna-hypertension
Product Packages
NDC Code 17089-347-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17089-347?
What are the uses for Guna-hypertension?
What are Guna-hypertension Active Ingredients?
- ARNICA MONTANA 12 [hp_X]/30mL
- FUMARIC ACID 3 [hp_X]/30mL
- GOLD 12 [hp_X]/30mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
- LEAD 12 [hp_X]/30mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
- 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.
- MELILOTUS 6 [hp_X]/30mL - A plant genus of the family FABACEAE. Molded yellow sweet clover hay, in which the coumarin of sweet clover is converted to DICOUMAROL, is the causative agent of a hemorrhagic disorder in cattle - "hemorrhagic sweet clover disease" and featured in the history of anticoagulant drug development.
- OLEA EUROPAEA FLOWER 3 [hp_X]/30mL
- PORK KIDNEY 6 [hp_X]/30mL
- RAUWOLFIA SERPENTINA 6 [hp_X]/30mL - A plant genus of the APOCYNACEAE or dogbane family. Alkaloids from plants in this genus have been used as tranquilizers and antihypertensive agents. RESERPINE is derived from R. serpentina.
- SODIUM PYRUVATE 3 [hp_X]/30mL
- SPIGELIA 6 [hp_X]/30mL - A plant family of the order Gentianales, subclass Asteridae, class Magnoliopsida. They have leaflike appendages at the base of the leafstalks, have terminal flower clusters. Petals have four or five overlapping lobes and the fruit is a capsule containing winged or wingless seeds.
- SUS SCROFA ADRENAL GLAND 200 [hp_X]/30mL
- SUS SCROFA DIENCEPHALON 6 [hp_X]/30mL
- UBIDECARENONE 3 [hp_X]/30mL
- VISCUM ALBUM FRUIT 3 [hp_X]/30mL
Which are Guna-hypertension UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- SUS SCROFA DIENCEPHALON (UNII: 23PJ4252VL)
- SUS SCROFA DIENCEPHALON (UNII: 23PJ4252VL) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- MELATONIN (UNII: JL5DK93RCL)
- MELATONIN (UNII: JL5DK93RCL) (Active Moiety)
- MELILOTUS (UNII: F22I9R6Q0X)
- MELILOTUS (UNII: F22I9R6Q0X) (Active Moiety)
- SODIUM PYRUVATE (UNII: POD38AIF08)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PYRUVIC ACID (UNII: 8558G7RUTR) (Active Moiety)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G) (Active Moiety)
- SPIGELIA (UNII: 467D26HS0B)
- SPIGELIA (UNII: 467D26HS0B) (Active Moiety)
- VISCUM ALBUM FRUIT (UNII: P83EQ521R3)
- VISCUM ALBUM FRUIT (UNII: P83EQ521R3) (Active Moiety)
Which are Guna-hypertension 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-hypertension?
* 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".