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  4. NDC Product Code: 59469-323 Apo-strum

NDC 59469-323 Apo-strum

Calcium Fluoride,Conium Maculatum Flowering Top,Lophophytum Leandrii,Hedera Helix - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59469-323?
  4. Apo-strum Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
59469-323
Proprietary Name:
Apo-strum
Non-Proprietary Name: [1]
Calcium Fluoride, Conium Maculatum Flowering Top, Lophophytum Leandrii, Hedera Helix Flowering Twig, Magnesium Carbonate, Cytisus Scoparius Flowering Top, Selenicereus Grandiflorus Whole, And Galium Aparine
Substance Name: [2]
Calcium Fluoride; Conium Maculatum Flowering Top; Cytisus Scoparius Flowering Top; Galium Aparine Whole; Hedera Helix Flowering Twig; Lophophytum Leandrii; Magnesium Carbonate; Selenicereus Grandiflorus Whole
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Pekana Naturheilmittel Gmbh
    Labeler Code:
    59469
    Product Label ID:
    9b4874fc-bb67-4627-8096-acedaeb81592
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    06-24-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 59469-323?

    The NDC code 59469-323 is assigned by the FDA to the product Apo-strum which is a human over the counter drug product labeled by Pekana Naturheilmittel Gmbh. The generic name of Apo-strum is calcium fluoride, conium maculatum flowering top, lophophytum leandrii, hedera helix flowering twig, magnesium carbonate, cytisus scoparius flowering top, selenicereus grandiflorus whole, and galium aparine. The product's dosage form is solution/ drops and is administered via oral form. The product is distributed in a single package with assigned NDC code 59469-323-10 1 bottle, glass in 1 box / 50 ml in 1 bottle, glass. 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 Apo-strum?

    This product is used as Regulative drops. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

    What are Apo-strum 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 Apo-strum UNII Codes?

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

    • CALCIUM FLUORIDE (UNII: O3B55K4YKI)
    • FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
    • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
    • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
    • LOPHOPHYTUM LEANDRII (UNII: 59150S2EOG)
    • LOPHOPHYTUM LEANDRII (UNII: 59150S2EOG) (Active Moiety)
    • HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM)
    • HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM) (Active Moiety)
    • MAGNESIUM CARBONATE (UNII: 0E53J927NA)
    • CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
    • CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666)
    • CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666) (Active Moiety)
    • SELENICEREUS GRANDIFLORUS WHOLE (UNII: X8H7HS7MRM)
    • SELENICEREUS GRANDIFLORUS WHOLE (UNII: X8H7HS7MRM) (Active Moiety)
    • GALIUM APARINE (UNII: Z4B6561488)
    • GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)

    Which are Apo-strum 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:

    Which are the Pharmacologic Classes for Apo-strum?

    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.

    * 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [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".