NDC 17089-299 Guna-allergy-prev
Ambrosia Artemisiifolia - Anguilla Rostrata Blood Serum - Arundo Pliniana Root - Black - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-299 - Guna-allergy-prev
Product Packages
NDC Code 17089-299-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17089-299?
What are the uses for Guna-allergy-prev?
What are Guna-allergy-prev Active Ingredients?
- AMBROSIA ARTEMISIIFOLIA 18 [hp_X]/30mL
- ANGUILLA ROSTRATA BLOOD SERUM 200 [hp_X]/30mL
- ARUNDO PLINIANA ROOT 18 [hp_X]/30mL
- ASCLEPIAS CURASSAVICA 6 [hp_X]/30mL
- BLACK CURRANT 1 [hp_X]/30mL
- CITRIC ACID MONOHYDRATE 6 [hp_X]/30mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
- HISTAMINE DIHYDROCHLORIDE 30 [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
- MANGANESE GLUCONATE 4 [hp_X]/30mL
- PARIETARIA OFFICINALIS 18 [hp_X]/30mL
- PHLEUM PRATENSE 18 [hp_X]/30mL
- SODIUM PYRUVATE 6 [hp_X]/30mL
- SODIUM SULFATE 200 [hp_X]/30mL
- SUCCINIC ACID 6 [hp_X]/30mL - A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
- SULFUR 30 [hp_X]/30mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- URTICA URENS 18 [hp_X]/30mL
- VIBURNUM OPULUS ROOT 3 g/30mL
- WYETHIA HELENIOIDES ROOT 18 [hp_X]/30mL
Which are Guna-allergy-prev UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (Active Moiety)
- ASCLEPIAS CURASSAVICA (UNII: JSZ93E47EP)
- ASCLEPIAS CURASSAVICA (UNII: JSZ93E47EP) (Active Moiety)
- BLACK CURRANT (UNII: 9755T40D11)
- BLACK CURRANT (UNII: 9755T40D11) (Active Moiety)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (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 12 (UNII: 7B590791ER)
- HUMAN INTERLEUKIN 12 (UNII: 7B590791ER) (Active Moiety)
- MANGANESE GLUCONATE (UNII: 9YY2F980SV)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- SODIUM PYRUVATE (UNII: POD38AIF08)
- PYRUVIC ACID (UNII: 8558G7RUTR) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PARIETARIA OFFICINALIS (UNII: 2C839WQ03N)
- PARIETARIA OFFICINALIS (UNII: 2C839WQ03N) (Active Moiety)
- PHLEUM PRATENSE (UNII: S7PW24BX20)
- PHLEUM PRATENSE (UNII: S7PW24BX20) (Active Moiety)
- ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U)
- ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U) (Active Moiety)
- SUCCINIC ACID (UNII: AB6MNQ6J6L)
- SUCCINIC ACID (UNII: AB6MNQ6J6L) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- VIBURNUM OPULUS ROOT (UNII: T1UG6H6805)
- VIBURNUM OPULUS ROOT (UNII: T1UG6H6805) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
Which are Guna-allergy-prev 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-allergy-prev?
- Acidifying Activity - [MoA] (Mechanism of Action)
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Interferon gamma - [EPC] (Established Pharmacologic Class)
- Interferon-gamma - [CS]
- Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Paramagnetic Contrast Agent - [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".