NDC 81488-002 Mineffect Skin Protectant

Alumina,Calcarea Silicata,Magnesia Sulphurica,Silicea,Sulphur,Titanium Metallicum,Zincum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
81488-002
Proprietary Name:
Mineffect Skin Protectant
Non-Proprietary Name: [1]
Alumina, Calcarea Silicata, Magnesia Sulphurica, Silicea, Sulphur, Titanium Metallicum, Zincum Metallicum
Substance Name: [2]
Aluminum Oxide; Calcium Silicate; Magnesium Sulfate Heptahydrate; Silicon Dioxide; Sulfur; Titanium; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Labeler Name: [5]
    Kadesh Incoporation Co,ltd
    Labeler Code:
    81488
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-01-2021
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 81488-002-04

    Package Description: 1 BOTTLE, SPRAY in 1 BOX / 118 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 81488-002?

    The NDC code 81488-002 is assigned by the FDA to the product Mineffect Skin Protectant which is a human over the counter drug product labeled by Kadesh Incoporation Co,ltd. The generic name of Mineffect Skin Protectant is alumina, calcarea silicata, magnesia sulphurica, silicea, sulphur, titanium metallicum, zincum metallicum. The product's dosage form is spray and is administered via topical form. The product is distributed in a single package with assigned NDC code 81488-002-04 1 bottle, spray in 1 box / 118 ml in 1 bottle, spray. 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 Skin Protectant?

    This product is used as Dry, Itchy SkinChaps, CracksItchy SkinItchy SkinOut-Breaks on SkinItchy Skin, EczemaEczemaEczema. • Temporarily protects and helps to relieve minor skin irritation and itching due to *rashes *eczema.• Temporarily protects minor *scratches *burns *chapped or cracked skin

    What are Mineffect Skin Protectant 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 7 [hp_X]/118mL - 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 6 [hp_X]/118mL
    • MAGNESIUM SULFATE HEPTAHYDRATE 7 [hp_X]/118mL
    • SILICON DIOXIDE 4 [hp_X]/118mL - 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.
    • SULFUR 4 [hp_X]/118mL - 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]/118mL - 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]/118mL - 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 Skin Protectant UNII Codes?

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

    Which are Mineffect Skin Protectant 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 Skin Protectant?

    * 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".