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  4. NDC Product Code: 62795-1131 Hendel Indigestion And Bloating

NDC 62795-1131 Hendel Indigestion And Bloating

Activated Charcoal,Strychnos Nux-vomica Seed,Silver Nitrate,Arsenic Trioxide,And Ipecac - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62795-1131?
  5. Hendel Indigestion And Bloating Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
62795-1131
Proprietary Name:
Hendel Indigestion And Bloating
Non-Proprietary Name: [1]
Activated Charcoal, Strychnos Nux-vomica Seed, Silver Nitrate, Arsenic Trioxide, And Ipecac
Substance Name: [2]
Activated Charcoal; Arsenic Trioxide; Ipecac; Silver Nitrate; Strychnos Nux-vomica Seed
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Medinatura Inc
    Labeler Code:
    62795
    Product Label ID:
    93d07ff6-886d-4bec-ba3e-7e3ba03c81ed
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-03-2018
    End Marketing Date: [10]
    09-30-2026
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    9 MM
    Imprint(s):
    LEAFMAN
    Score:
    1

    Product Packages

    NDC Code 62795-1131-2

    Package Description: 100 TABLET in 1 BOTTLE

    Product Details

    What is NDC 62795-1131?

    The NDC code 62795-1131 is assigned by the FDA to the product Hendel Indigestion And Bloating which is a human over the counter drug product labeled by Medinatura Inc. The generic name of Hendel Indigestion And Bloating is activated charcoal, strychnos nux-vomica seed, silver nitrate, arsenic trioxide, and ipecac. The product's dosage form is tablet and is administered via oral form. The product is distributed in a single package with assigned NDC code 62795-1131-2 100 tablet in 1 bottle . 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 Hendel Indigestion And Bloating?

    Indigestion & Bloating Relief For the temporary relief of:• Indigestion• Feeling of fullness• Nausea

    What are Hendel Indigestion And Bloating 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.
    • ACTIVATED CHARCOAL 3 [hp_X]/1
    • ARSENIC TRIOXIDE 12 [hp_X]/1 - 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.
    • IPECAC 6 [hp_X]/1 - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
    • SILVER NITRATE 6 [hp_X]/1 - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
    • STRYCHNOS NUX-VOMICA SEED 3 [hp_X]/1

    Which are Hendel Indigestion And Bloating UNII Codes?

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

    Which are Hendel Indigestion And Bloating 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 Hendel Indigestion And Bloating?

    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.

    [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".