Echinacea Tablet, Orally Disintegrating
NDC 60986-2020
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Echinacea (echinacea angustifolia, hamammelis virginiana, calcarea phosphorica, hydrastis canadanesis, senega officinalis, silicea, conium, aurum muriaticum natronatum, calcarea carbonica, fucus vesiculosus, lachesis mutus) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Marco Pharma International Llc.. This medication is typically used as a blood coagulation factor [epc]. It is supplied as a white tablet, orally disintegrating for oral administration. This product entry covers the primary NDC 60986-2020 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
60986-2020
Proprietary Name:
Echinacea
Non-Proprietary Name: [1]
Echinacea Angustifolia, Hamammelis Virginiana, Calcarea Phosphorica, Hydrastis Canadanesis, Senega Officinalis, Silicea, Conium, Aurum Muriaticum Natronatum, Calcarea Carbonica, Fucus Vesiculosus, Lachesis Mutus
Substance Name: [2]
Conium Maculatum Flowering Top; Echinacea Angustifolia; Fucus Vesiculosus; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Lachesis Muta Venom; Oyster Shell Calcium Carbonate, Crude; Polygala Senega Root; Silicon Dioxide; Sodium Tetrachloroaurate; Tribasic Calcium Phosphate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Tablet, Orally Disintegrating
- A solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
60986
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
03-01-1992
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Product Characteristics
Color(s):
WHITE (C48325 - LIGHT BROWN)
Shape:
CAPSULE (C48336)
Size(s):
12 MM
Score:
1
Code Structure Chart
Product Details
What is NDC 60986-2020?
The NDC code 60986-2020 is assigned by the FDA to the product Echinacea. It is commonly known by its generic name, echinacea angustifolia, hamammelis virginiana, calcarea phosphorica, hydrastis canadanesis, senega officinalis, silicea, conium, aurum muriaticum natronatum, calcarea carbonica, fucus vesiculosus, lachesis mutus. This pharmaceutical product is labeled by Marco Pharma International Llc. and is currently categorized as listed product. The medication is a tablet, orally disintegrating administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 60986-2020-2. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
This product is used as FOR TEMPORARY RELIEF OF SORE THROATS AND LYMPHATIC INFLAMMATION.
What are Active Ingredients of this product?
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.
- 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
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299)
- TETRACHLOROAURATE ION (UNII: ZNL6IP5PJX) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
Which are the Inactive Ingredients associated 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:
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- LACTOSE (UNII: J2B2A4N98G)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
