NDC 17089-260 Guna-diur
Amiloride - Apis Mellifera - Berberis Vulgaris Fruit - Hieracium Pilosella Flowering Top - - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17089-260?
What are the uses for Guna-diur?
What are Guna-diur Active Ingredients?
- AMILORIDE 4 [hp_X]/30mL - A pyrazine compound inhibiting SODIUM reabsorption through SODIUM CHANNELS in renal EPITHELIAL CELLS. This inhibition creates a negative potential in the luminal membranes of principal cells, located in the distal convoluted tubule and collecting duct. Negative potential reduces secretion of potassium and hydrogen ions. Amiloride is used in conjunction with DIURETICS to spare POTASSIUM loss. (From Gilman et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 9th ed, p705)
- APIS MELLIFERA 2 [hp_X]/30mL
- BERBERIS VULGARIS FRUIT .3 g/30mL
- HIERACIUM PILOSELLA FLOWERING TOP .3 g/30mL
- HYDROCHLOROTHIAZIDE 4 [hp_X]/30mL - A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.
- SOLIDAGO VIRGAUREA FLOWERING TOP .3 g/30mL
- SPIRONOLACTONE 4 [hp_X]/30mL - A potassium sparing diuretic that acts by antagonism of aldosterone in the distal renal tubules. It is used mainly in the treatment of refractory edema in patients with congestive heart failure, nephrotic syndrome, or hepatic cirrhosis. Its effects on the endocrine system are utilized in the treatments of hirsutism and acne but they can lead to adverse effects. (From Martindale, The Extra Pharmacopoeia, 30th ed, p827)
- SUS SCROFA PITUITARY GLAND 12 [hp_X]/30mL
Which are Guna-diur UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMILORIDE (UNII: 7DZO8EB0Z3)
- AMILORIDE (UNII: 7DZO8EB0Z3) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3)
- BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3) (Active Moiety)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
- HIERACIUM PILOSELLA FLOWERING TOP (UNII: 08A7Y81S1P)
- HIERACIUM PILOSELLA FLOWERING TOP (UNII: 08A7Y81S1P) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- SPIRONOLACTONE (UNII: 27O7W4T232)
- SPIRONOLACTONE (UNII: 27O7W4T232) (Active Moiety)
Which are Guna-diur 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-diur?
- Aldosterone Antagonist - [EPC] (Established Pharmacologic Class)
- Aldosterone Antagonists - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Decreased Renal K+ Excretion - [PE] (Physiologic Effect)
- Increased Diuresis - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Potassium-sparing Diuretic - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Thiazide Diuretic - [EPC] (Established Pharmacologic Class)
- Thiazides - [CS]
* 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".