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  4. NDC Product Code: 57520-1365 Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis

NDC 57520-1365 Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis

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

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57520-1365?
  4. Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

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.

Get all the details for National Drug Code (NDC) 57520-1365 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
57520-1365
Proprietary Name:
Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis
Non-Proprietary Name: [1]
Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis
Substance Name: [2]
Arsenic Trioxide; Berberis Vulgaris Root Bark; Iris Versicolor Root; Juniper Berry; Phytolacca Americana Root; Solidago Virgaurea Flowering Top; Taraxacum Officinale; Thuja Occidentalis Leafy Twig
NDC Directory Status:
Bulk Ingredient - Animal Drug
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
Product Label ID:
58969530-a160-42be-9a38-67a521d07ecb
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]
12-12-2018
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57520-1365?

The NDC code 57520-1365 is assigned by the FDA to the UNFINISHED product Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis which is bulk ingredient - animal drug product labeled by Apotheca Company. The generic name of Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis is juniperus communis, solidago virgaurea, taraxacum officinale, phytolacca decandra, arsenicum album, berberis vulgaris, iris versicolor, thuja occidentalis. The product's dosage form is liquid. The product is distributed in a single package with assigned NDC code 57520-1365-1 3785 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 the uses for Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis?

TO BE DETERMINED BY FINAL PROCESSOR

What are Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis 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.

Which are Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis UNII Codes?

The UNII codes for the active ingredients in this product are:

  • JUNIPER BERRY (UNII: O84B5194RL)
  • JUNIPER BERRY (UNII: O84B5194RL) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • TARAXACUM OFFICINALE (UNII: 39981FM375)
  • TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)

Which are Juniperus Communis, Solidago Virgaurea, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Berberis Vulgaris, Iris Versicolor, Thuja Occidentalis 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:

* Please review the disclaimer below.

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.

[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, 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".

[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.