NDC 60295-0101 Echinacea Angustifolia, Hamammelis Virginiana, Calcarea Phosphorica, Hydrastis Canadanesis, Senega Officinalis, Silicea, Conium, Aurum Muriaticum Natronatum, Calcarea Carbonica, Fucus Vesiculosus, Lachesis Mutus
Tablet, Orally Disintegrating - View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 60295-0101?
What are Echinacea Angustifolia, Hamammelis Virginiana, Calcarea Phosphorica, Hydrastis Canadanesis, Senega Officinalis, Silicea, Conium, Aurum Muriaticum Natronatum, Calcarea Carbonica, Fucus Vesiculosus, Lachesis Mutus Active Ingredients?
- CONIUM MACULATUM FLOWERING TOP 4 [hp_X]/1
- ECHINACEA ANGUSTIFOLIA 1 [hp_X]/1 - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- FUCUS VESICULOSUS 5 [hp_X]/1 - 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.
- GOLDENSEAL 4 [hp_X]/1
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 2 [hp_X]/1
- LACHESIS MUTA VENOM 8 [hp_X]/1
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 5 [hp_X]/1
- POLYGALA SENEGA ROOT 4 [hp_X]/1
- SILICON DIOXIDE 4 [hp_X]/1 - 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 TETRACHLOROAURATE 5 [hp_X]/1
- TRIBASIC CALCIUM PHOSPHATE 3 [hp_X]/1
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[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.
[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".
[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.