Meb Puri-mega Liquid
NDC 81488-012

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 81488-012?
  4. Meb Puri-mega Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Meb Puri-mega is a UNAPPROVED HOMEOPATHIC-approved product labeled by Kadesh Incoporation Co,ltd. This medication is typically used as a calculi dissolution agent [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 81488-012 and 2 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
81488-012
Proprietary Name:
Meb Puri-mega
Non-Proprietary Name: [1]
Meb Puri-mega
Substance Name: [2]
Calcium Fluoride; Ferric Chloride Hexahydrate; Ferrosoferric Phosphate; Magnesium Chloride; Magnesium Sulfate Heptahydrate; Phosphorus; Silicon Dioxide; Sodium Nitrate; Sulfur; Titanium; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Kadesh Incoporation Co,ltd
Labeler Code:
81488
Product Label ID:
018125f2-ad4b-b38a-e063-6294a90a7f6e
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
08-18-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 81488-012?

The NDC code 81488-012 is assigned by the FDA to the product Meb Puri-mega. This pharmaceutical product is labeled by Kadesh Incoporation Co,ltd and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in 2 different package configurations. The associated package NDC(s) include: 81488-012-03, 81488-012-10. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

MEB Puri-Mega“Potent mineral concentrate with exceptional health benefits. Offers unparalleled support for overall well-being, including asthma, immune deficiency, rhinitis, diabetes and more.”Usage:Puri-Mega is a potent mineral concentrate enriched with various health benefits. Extracted from beneficial minerals known for their exceptional absorbability in the human body, this health blend offers unparalleled support for overall well-being. The natural healing and preventive properties of Puriton Mineral, a 100% pure mineral extract sourced from nature offer exceptional effectiveness in conditions such as asthma, immune deficiency, stomach disease, rhinitis, and diabetes.

What are Active Ingredients of this product?

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.
  • CALCIUM FLUORIDE 6 [hp_X]/300mL - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
  • FERRIC CHLORIDE HEXAHYDRATE 7 [hp_X]/300mL
  • FERROSOFERRIC PHOSPHATE 7 [hp_X]/300mL
  • MAGNESIUM CHLORIDE 7 [hp_X]/300mL - 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.
  • MAGNESIUM SULFATE HEPTAHYDRATE 7 [hp_X]/300mL
  • PHOSPHORUS 6 [hp_X]/300mL - 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]/300mL - 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 5 [hp_X]/300mL
  • SULFUR 4 [hp_X]/300mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
  • TITANIUM 7 [hp_X]/300mL - A dark-gray, metallic element of widespread distribution but occurring in small amounts with atomic number, 22, atomic weight, 47.867 and symbol, Ti; specific gravity, 4.5; used for fixation of fractures.
  • ZINC 8 [hp_X]/300mL - 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 the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 of this product?

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 & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".