NDC 59469-102 Apo-stom

Antimony Trisulfide,Atropa Bella-donna Flowering Top,Colchicum Autumnale Bulb,Citrullus - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
59469-102
Proprietary Name:
Apo-stom
Non-Proprietary Name: [1]
Antimony Trisulfide, Atropa Bella-donna Flowering Top, Colchicum Autumnale Bulb, Citrullus Colocynthis Fruit Pulp, Sodium Phosphate, Strychnos Nux-vomica Seed, Robinia Pseudoacacia Bark, And Achillea Millefolium Flowering Top
Substance Name: [2]
Achillea Millefolium Flowering Top; Antimony Trisulfide; Atropa Bella-donna Flowering Top; Citrullus Colocynthis Fruit Pulp; Colchicum Autumnale Bulb; Robinia Pseudoacacia Bark; Sodium Phosphate; Strychnos Nux-vomica Seed
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 Code:
    59469
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-11-2008
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 59469-102?

    The NDC code 59469-102 is assigned by the FDA to the product Apo-stom which is a human over the counter drug product labeled by Pekana Naturheilmittel Gmbh. The generic name of Apo-stom is antimony trisulfide, atropa bella-donna flowering top, colchicum autumnale bulb, citrullus colocynthis fruit pulp, sodium phosphate, strychnos nux-vomica seed, robinia pseudoacacia bark, and achillea millefolium flowering top. 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 59469-102-10 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-stom?

    This product is used as For support of stomach and intestinal function. 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-stom 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-stom UNII Codes?

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

    • ANTIMONY TRISULFIDE (UNII: F79059A38U)
    • ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
    • ATROPA BELLA-DONNA FLOWERING TOP (UNII: B26WXN5GZJ)
    • ATROPA BELLA-DONNA FLOWERING TOP (UNII: B26WXN5GZJ) (Active Moiety)
    • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
    • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
    • SODIUM PHOSPHATE (UNII: SE337SVY37)
    • PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
    • ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY)
    • ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY) (Active Moiety)
    • ACHILLEA MILLEFOLIUM FLOWERING TOP (UNII: 55862Q3XEU)
    • ACHILLEA MILLEFOLIUM FLOWERING TOP (UNII: 55862Q3XEU) (Active Moiety)

    Which are Apo-stom 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-stom?

    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".