NDC 17089-460 Guna Matrix Detox
Sodium Sulfate - Podophyllum Peltatum Root - Solidago Virgaurea Flowering Top - Apis - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17089-460?
What are the uses for Guna Matrix Detox?
What are Guna Matrix Detox Active Ingredients?
- CONIUM MACULATUM FLOWERING TOP 3 [hp_X]/30mL
- FUCUS VESICULOSUS 6 [hp_X]/30mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
- GALIUM APARINE WHOLE 4 [hp_X]/30mL
- GRAPHITE 12 [hp_X]/30mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- MALIC ACID 6 [hp_X]/30mL
- MYOSOTIS ARVENSIS 4 [hp_X]/30mL
- RANCID BEEF 12 [hp_X]/30mL
- SILICON DIOXIDE 8 [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.
- SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL
- SODIUM PYRUVATE 3 [hp_X]/30mL
- SODIUM SULFATE 12 [hp_X]/30mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 2 [hp_X]/30mL
- SUS SCROFA VEIN 6 [hp_X]/30mL
- THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/30mL
- URTICA URENS WHOLE 6 [hp_X]/30mL
Which are Guna Matrix Detox UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- URTICA URENS WHOLE (UNII: IHN2NQ5OF9)
- URTICA URENS WHOLE (UNII: IHN2NQ5OF9) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- SODIUM PYRUVATE (UNII: POD38AIF08)
- PYRUVIC ACID (UNII: 8558G7RUTR) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- SUS SCROFA VEIN (UNII: 2510RH3I89)
- SUS SCROFA VEIN (UNII: 2510RH3I89) (Active Moiety)
- GALIUM APARINE WHOLE (UNII: Z4B6561488)
- GALIUM APARINE WHOLE (UNII: Z4B6561488) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
- MALIC ACID (UNII: 817L1N4CKP)
- MALIC ACID (UNII: 817L1N4CKP) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Guna Matrix Detox 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 Matrix Detox?
* 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".