NDC 17089-419 Guna-rhino Nose
Apis Mellifera - Aralia Racemosa Root - Ascorbic Acid - Black Currant - Copper - Euphorbia - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-419 - Guna-rhino Nose
Product Packages
NDC Code 17089-419-23
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 17089-419?
What are the uses for Guna-rhino Nose?
What are Guna-rhino Nose Active Ingredients?
- APIS MELLIFERA 12 [hp_X]/30mL
- ARALIA RACEMOSA ROOT 1 [hp_X]/30mL
- ASCORBIC ACID 2 [hp_X]/30mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- BLACK CURRANT 1 [hp_X]/30mL
- COPPER 4 [hp_X]/30mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- EUPHORBIA RESINIFERA RESIN 4 [hp_X]/30mL
- EUROPEAN ELDERBERRY 2 [hp_X]/30mL
- HELIANTHEMUM CANADENSE 4 [hp_X]/30mL
- HISTAMINE DIHYDROCHLORIDE 200 [hp_X]/30mL - 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.
- HUMAN INTERLEUKIN 12 4 [hp_C]/30mL
- INTERFERON GAMMA-1B 4 [hp_C]/30mL
- INTERLEUKIN-10 4 [hp_C]/30mL - A cytokine produced by a variety of cell types, including T-LYMPHOCYTES; MONOCYTES; DENDRITIC CELLS; and EPITHELIAL CELLS that exerts a variety of effects on immunoregulation and INFLAMMATION. Interleukin-10 combines with itself to form a homodimeric molecule that is the biologically active form of the protein.
- MANGANESE GLUCONATE 4 [hp_X]/30mL
- MELILOTUS 3 [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.
- ONION 8 [hp_X]/30mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PLANTAGO MAJOR 2 [hp_X]/30mL
- ROSA CANINA FRUIT 1 [hp_X]/30mL
- SILVER NITRATE 10 [hp_X]/30mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
Which are Guna-rhino Nose UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- BLACK CURRANT (UNII: 9755T40D11)
- BLACK CURRANT (UNII: 9755T40D11) (Active Moiety)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- INTERFERON GAMMA-1B (UNII: 21K6M2I7AG)
- INTERFERON GAMMA-1B (UNII: 21K6M2I7AG) (Active Moiety)
- HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) (UNII: 9SC4O216V9)
- HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) (UNII: 9SC4O216V9) (Active Moiety)
- HUMAN INTERLEUKIN 12 (UNII: 7B590791ER)
- HUMAN INTERLEUKIN 12 (UNII: 7B590791ER) (Active Moiety)
- MANGANESE GLUCONATE (UNII: 9YY2F980SV)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- MELILOTUS (UNII: F22I9R6Q0X)
- MELILOTUS (UNII: F22I9R6Q0X) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3) (Active Moiety)
- EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
- EUROPEAN ELDERBERRY (UNII: BQY1UBX046) (Active Moiety)
Which are Guna-rhino Nose 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:
- ORANGE JUICE (UNII: 5A9KE2L9L3)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
Which are the Pharmacologic Classes for Guna-rhino Nose?
- Allergens - [CS]
- Allergens - [CS]
- Ascorbic Acid - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Interferon gamma - [EPC] (Established Pharmacologic Class)
- Interferon-gamma - [CS]
- Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
- Vitamin C - [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".