NDC 17089-472 Guna Sinus Plus
Althaea Officinalis Leaf - Calcium Sulfide - Copper - Drimia Maritima Bulb - Echinacea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-472 - Guna Sinus Plus
Product Packages
NDC Code 17089-472-23
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 17089-472?
What are the uses for Guna Sinus Plus?
What are Guna Sinus Plus Active Ingredients?
- ALTHAEA OFFICINALIS LEAF 2 [hp_X]/30mL
- ASCORBIC ACID 3 [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.
- CALCIUM SULFIDE 6 [hp_X]/30mL
- COPPER 8 [hp_X]/30mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- DRIMIA MARITIMA BULB 12 [hp_X]/30mL
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/30mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- HYDRASTIS CANADENSIS WHOLE 6 [hp_X]/30mL
- LOBARIA PULMONARIA 2 [hp_X]/30mL
- MANGANESE 8 [hp_X]/30mL - A trace element with atomic symbol Mn, atomic number 25, and atomic weight 54.94. It is concentrated in cell mitochondria, mostly in the pituitary gland, liver, pancreas, kidney, and bone, influences the synthesis of mucopolysaccharides, stimulates hepatic synthesis of cholesterol and fatty acids, and is a cofactor in many enzymes, including arginase and alkaline phosphatase in the liver. (From AMA Drug Evaluations Annual 1992, p2035)
- MERCURIC SULFIDE 8 [hp_X]/30mL
- ONION 6 [hp_X]/30mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PLANTAGO MAJOR WHOLE 2 [hp_X]/30mL
- POTASSIUM DICHROMATE 6 [hp_X]/30mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
- PULSATILLA VULGARIS 6 [hp_X]/30mL
- SILICON DIOXIDE 6 [hp_X]/30mL - 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.
- SILVER NITRATE 10 [hp_X]/30mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
- SINUSITISINUM 12 [hp_X]/30mL
- SUS SCROFA NASAL MUCOSA 6 [hp_X]/30mL
Which are Guna Sinus Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- ALTHAEA OFFICINALIS LEAF (UNII: E2QQV92338)
- ALTHAEA OFFICINALIS LEAF (UNII: E2QQV92338) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) (Active Moiety)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- MANGANESE (UNII: 42Z2K6ZL8P)
- MANGANESE (UNII: 42Z2K6ZL8P) (Active Moiety)
- MERCURIC SULFIDE (UNII: ZI0T668SF1)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY)
- SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SINUSITISINUM (UNII: B575563DM5)
- SINUSITISINUM (UNII: B575563DM5) (Active Moiety)
- PLANTAGO MAJOR WHOLE (UNII: W2469WNO6U)
- PLANTAGO MAJOR WHOLE (UNII: W2469WNO6U) (Active Moiety)
- DRIMIA MARITIMA BULB (UNII: 3629601H5D)
- DRIMIA MARITIMA BULB (UNII: 3629601H5D) (Active Moiety)
Which are Guna Sinus Plus 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:
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
Which are the Pharmacologic Classes for Guna Sinus Plus?
- Allergens - [CS]
- Ascorbic Acid - [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)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Non-Standardized Food 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".