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  4. NDC Product Code: 81488-008 Mineffect Acid Indigestion And Heartburn Relief

NDC 81488-008 Mineffect Acid Indigestion And Heartburn Relief

Alumina,Calcarea Silicata,Ferrum Metallicum,Ferrum Phosphoricum,Magnesia Muriatica,Natrum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81488-008?
  4. Mineffect Acid Indigestion And Heartburn Relief Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
81488-008
Proprietary Name:
Mineffect Acid Indigestion And Heartburn Relief
Non-Proprietary Name: [1]
Alumina, Calcarea Silicata, Ferrum Metallicum, Ferrum Phosphoricum, Magnesia Muriatica, Natrum Nitricum, Phosphorus, Silicea, Zincum Metallicum
Substance Name: [2]
Aluminum Oxide; Calcium Silicate; Ferrosoferric Phosphate; Iron; Magnesium Chloride; Phosphorus; Silicon Dioxide; Sodium Nitrate; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE 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.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Kadesh Incoporation Co,ltd
    Labeler Code:
    81488
    Product Label ID:
    048367ff-a9bb-46a3-a835-aa3ab391eee4
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-21-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 81488-008?

    The NDC code 81488-008 is assigned by the FDA to the product Mineffect Acid Indigestion And Heartburn Relief which is a human over the counter drug product labeled by Kadesh Incoporation Co,ltd. The generic name of Mineffect Acid Indigestion And Heartburn Relief is alumina, calcarea silicata, ferrum metallicum, ferrum phosphoricum, magnesia muriatica, natrum nitricum, phosphorus, silicea, zincum metallicum. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 81488-008-01 1 bottle in 1 box / 30 ml 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 Mineffect Acid Indigestion And Heartburn Relief?

    This product is used as HeartburnVomitingVomitingAcid IndigestionAcid IndigestionStomachacheVomitingAcid IndigestionHeartburn. Temporary relieves the symptoms of heartburn, upset stomach, acid indigestion and bloating.

    What are Mineffect Acid Indigestion And Heartburn Relief 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.
    • ALUMINUM OXIDE 5 [hp_X]/30mL - 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.
    • CALCIUM SILICATE 5 [hp_X]/30mL
    • FERROSOFERRIC PHOSPHATE 7 [hp_X]/30mL
    • IRON 7 [hp_X]/30mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
    • MAGNESIUM CHLORIDE 4 [hp_X]/30mL - Magnesium chloride. An inorganic compound consisting of one magnesium and two chloride ions. The compound is used in medicine as a source of magnesium ions, which are essential for many cellular activities. It has also been used as a cathartic and in alloys.
    • PHOSPHORUS 6 [hp_X]/30mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
    • SILICON DIOXIDE 4 [hp_X]/30mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
    • SODIUM NITRATE 4 [hp_X]/30mL
    • ZINC 8 [hp_X]/30mL - 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.

    Which are Mineffect Acid Indigestion And Heartburn Relief UNII Codes?

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

    Which are Mineffect Acid Indigestion And Heartburn Relief 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 Mineffect Acid Indigestion And Heartburn Relief?

    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.

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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.

    [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".