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NDC 79596-090 Too Faced Tinted Beauty Balm Spf-20

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79596-090?
  4. Too Faced Tinted Beauty Balm Spf-20 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:
79596-090
Proprietary Name:
Too Faced Tinted Beauty Balm Spf-20
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Too Faced Cosmetics
Labeler Code:
79596
Product Label ID:
b9685e2f-4009-45c8-ad09-03195dca879f
Start Marketing Date: [9]
12-14-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79596-090-22

Package Description: 1 TUBE in 1 BOX / 45 mL in 1 TUBE (79596-090-21)

Product Details

What is NDC 79596-090?

The NDC code 79596-090 is assigned by the FDA to the product Too Faced Tinted Beauty Balm Spf-20 which is product labeled by Too Faced Cosmetics. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79596-090-22 1 tube in 1 box / 45 ml in 1 tube (79596-090-21). 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 Too Faced Tinted Beauty Balm Spf-20?

USEHELPS PREVENT SUNBURN

Which are Too Faced Tinted Beauty Balm Spf-20 UNII Codes?

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

Which are Too Faced Tinted Beauty Balm Spf-20 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".