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  4. NDC Product Code: 80449-004 Sweat Gleam On Mineral Illuminator Spf 25

NDC 80449-004 Sweat Gleam On Mineral Illuminator Spf 25

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80449-004?
  4. Sweat Gleam On Mineral Illuminator Spf 25 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:
80449-004
Proprietary Name:
Sweat Gleam On Mineral Illuminator Spf 25
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sweat Cosmetics, Inc.
Labeler Code:
80449
Product Label ID:
dfe96f0a-92e3-47a3-82d4-d9e2b52b108d
Start Marketing Date: [9]
07-27-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80449-004-01

Package Description: 1 CONTAINER in 1 BOX / 2.7 g in 1 CONTAINER

NDC Code 80449-004-02

Package Description: 1 CONTAINER in 1 BOX / 2.7 g in 1 CONTAINER

Product Details

What is NDC 80449-004?

The NDC code 80449-004 is assigned by the FDA to the product Sweat Gleam On Mineral Illuminator Spf 25 which is product labeled by Sweat Cosmetics, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 80449-004-01 1 container in 1 box / 2.7 g in 1 container, 80449-004-02 1 container in 1 box / 2.7 g in 1 container. 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 Sweat Gleam On Mineral Illuminator Spf 25?

This product is used as Sunscreen

Which are Sweat Gleam On Mineral Illuminator Spf 25 UNII Codes?

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

Which are Sweat Gleam On Mineral Illuminator Spf 25 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".