NDC 17089-293 Guna-bowel
Aloe - Aluminum Oxide - Bryonia Alba Root - Chelidonium Majus - Cholecalciferol - - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-293 - Guna-bowel
Product Packages
NDC Code 17089-293-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17089-293?
What are the uses for Guna-bowel?
What are Guna-bowel Active Ingredients?
- ALOE 2 [hp_X]/30mL - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
- ALUMINUM OXIDE 6 [hp_X]/30mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
- BRYONIA ALBA ROOT 6 [hp_X]/30mL
- CHELIDONIUM MAJUS 2 [hp_X]/30mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- CHOLECALCIFEROL 2 [hp_X]/30mL - Derivative of 7-dehydroxycholesterol formed by ULTRAVIOLET RAYS breaking of the C9-C10 bond. It differs from ERGOCALCIFEROL in having a single bond between C22 and C23 and lacking a methyl group at C24.
- COLLINSONIA 2 [hp_X]/30mL
- FRANGULA ALNUS BARK 2 [hp_X]/30mL
- NIACIN 2 [hp_X]/30mL - A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties.
- PANTOTHENIC ACID 2 [hp_X]/30mL - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
- POTASSIUM CARBONATE 6 [hp_X]/30mL
- RHUBARB 2 [hp_X]/30mL
- SILYBUM MARIANUM SEED 2 [hp_X]/30mL
- SKATOLE 10 [hp_X]/30mL
- SODIUM CARBONATE 6 [hp_X]/30mL
- STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/30mL
- SUS SCROFA COLON 12 [hp_X]/30mL
- SUS SCROFA RECTUM 12 [hp_X]/30mL
- TARAXACUM OFFICINALE 2 [hp_X]/30mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- THIAMINE 4 [hp_X]/30mL - 3-((4-Amino-2-methyl-5-pyrimidinyl)methyl)-5-(2- hydroxyethyl)-4-methylthiazolium chloride.
Which are Guna-bowel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- COLLINSONIA (UNII: J9BTD5377V)
- COLLINSONIA (UNII: J9BTD5377V) (Active Moiety)
- SUS SCROFA COLON (UNII: 94J255A0UC)
- SUS SCROFA COLON (UNII: 94J255A0UC) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- SUS SCROFA RECTUM (UNII: QV1358E70N)
- SUS SCROFA RECTUM (UNII: QV1358E70N) (Active Moiety)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R) (Active Moiety)
- RHUBARB (UNII: G280W4MW6E)
- RHUBARB (UNII: G280W4MW6E) (Active Moiety)
- SKATOLE (UNII: 9W945B5H7R)
- SKATOLE (UNII: 9W945B5H7R) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE (UNII: X66NSO3N35) (Active Moiety)
Which are Guna-bowel 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-bowel?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Nicotinic Acid - [EPC] (Established Pharmacologic Class)
- Nicotinic Acids - [CS]
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Vitamin D - [CS]
- Vitamin D - [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".