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  4. NDC Product Code: 57520-1403 Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum

NDC 57520-1403 Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum

Liquid - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57520-1403?
  4. Active Ingredients

Product Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.
NDC Product Code:
57520-1403
Proprietary Name:
Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum
Non-Proprietary Name: [1]
Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum
Substance Name: [2]
Aconitum Napellus Whole; Aluminum Oxide; Arsenic Trioxide; Euphrasia Stricta; Nutmeg; Sodium Chloride; Zinc
NDC Directory Status:
Drug For Further Processing
Product Type: [3]
UNFINISHED PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Labeler Name: [5]
Apotheca Company
Labeler Code:
57520
Marketing Category: [8]
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date: [9]
10-13-2020
End Marketing Date: [10]
10-22-2025
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57520-1403?

The NDC code 57520-1403 is assigned by the FDA to the UNFINISHED product Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum which is drug for further processing product labeled by Apotheca Company. The generic name of Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum is euphrasia officinalis, nux moschata, zincum metallicum, arsenicum album, alumina, aconitum napellus, natrum muriaticum. The product's dosage form is liquid. The product is distributed in a single package with assigned NDC code 57520-1403-4 3840 ml in 1 jug . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are Euphrasia Officinalis, Nux Moschata, Zincum Metallicum, Arsenicum Album, Alumina, Aconitum Napellus, Natrum Muriaticum Active Ingredients?

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.
  • ACONITUM NAPELLUS WHOLE 12 [hp_C]/mL
  • ALUMINUM OXIDE 11 [hp_X]/mL - 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.
  • ARSENIC TRIOXIDE 9 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
  • EUPHRASIA STRICTA 2 [hp_X]/mL
  • NUTMEG 3 [hp_X]/mL
  • SODIUM CHLORIDE 12 [hp_C]/mL - A ubiquitous sodium salt that is commonly used to season food.
  • ZINC 8 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

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Product Footnotes

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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.