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  4. NDC Product Code: 52667-008 Bb Shade 20 Aglow Spf15

NDC 52667-008 Bb Shade 20 Aglow Spf15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52667-008?
  4. Bb Shade 20 Aglow Spf15 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:
52667-008
Proprietary Name:
Bb Shade 20 Aglow Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Purity Cosmetics
Labeler Code:
52667
Product Label ID:
60df03a9-25ea-d5d0-e053-2991aa0a0be0
Start Marketing Date: [9]
12-21-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 52667-008?

The NDC code 52667-008 is assigned by the FDA to the product Bb Shade 20 Aglow Spf15 which is product labeled by Purity Cosmetics. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52667-008-30 30 ml in 1 bottle . 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 Bb Shade 20 Aglow Spf15?

BB cream is a moisturizing skincare/makeup hybrid that is your primer, SPF, soothing treatment, concealer and foundation in one. After your normal skin care regimen, apply and blend well.

Which are Bb Shade 20 Aglow Spf15 UNII Codes?

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

Which are Bb Shade 20 Aglow Spf15 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".