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  4. NDC Product Code: 75936-280 Mineral Mattescreen Broad Spectrum Spf 40

NDC 75936-280 Mineral Mattescreen Broad Spectrum Spf 40

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75936-280?
  4. Mineral Mattescreen Broad Spectrum Spf 40 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75936-280
Proprietary Name:
Mineral Mattescreen Broad Spectrum Spf 40
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Taylor James
Labeler Code:
75936
Product Label ID:
64cfceb8-8ec4-61bd-e053-2991aa0a9507
Start Marketing Date: [9]
02-09-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 75936-280?

The NDC code 75936-280 is assigned by the FDA to the product Mineral Mattescreen Broad Spectrum Spf 40 which is product labeled by Taylor James. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 75936-280-01 5 ml in 1 tube , 75936-280-02 45 ml in 1 box , 75936-280-03 15 ml in 1 tube . 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 Mineral Mattescreen Broad Spectrum Spf 40?

This product is used as UsesHelps prevent SunburnIf used as directed with other sun protection ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Which are Mineral Mattescreen Broad Spectrum Spf 40 UNII Codes?

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

Which are Mineral Mattescreen Broad Spectrum Spf 40 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:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".