NDC 57520-1493 Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum
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Product Information
- 57520 - Apotheca Company
- 57520-1493 -
Product Packages
NDC Code 57520-1493-4
Package Description: 2350 kg in 1 CONTAINER
Product Details
What is NDC 57520-1493?
What are Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum Active Ingredients?
- ACHILLEA MILLEFOLIUM WHOLE 12 [hp_X]/kg
- ARNICA MONTANA WHOLE 1 [hp_X]/kg
- ATROPA BELLADONNA 30 [hp_X]/kg - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BELLIS PERENNIS WHOLE 12 [hp_X]/kg
- CALCIUM FLUORIDE 30 [hp_X]/kg - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
- CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/kg
- COMFREY ROOT 6 [hp_X]/kg
- FERROSOFERRIC PHOSPHATE 30 [hp_X]/kg
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 1 [hp_X]/kg
- HYPERICUM PERFORATUM WHOLE 1 [hp_X]/kg
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/kg
- RHODODENDRON TOMENTOSUM LEAFY TWIG 12 [hp_X]/kg
- RUTA GRAVEOLENS FLOWERING TOP 30 [hp_X]/kg
- SODIUM SULFATE 30 [hp_C]/kg
- SULFURIC ACID 12 [hp_X]/kg
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/kg
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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.