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  4. NDC Product Code: 64141-001 Bobbi Brown Skin Foundation Spf 15

NDC 64141-001 Bobbi Brown Skin Foundation Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64141-001?
  4. Bobbi Brown Skin Foundation Spf 15 Uses
  5. Active 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:
64141-001
Proprietary Name:
Bobbi Brown Skin Foundation Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bobbi Brown Professional Cosmetics Inc
Labeler Code:
64141
Product Label ID:
03b11d23-950e-40db-a553-3ab4aa17a246
Start Marketing Date: [9]
06-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64141-001-01

Package Description: 1 BOTTLE, GLASS in 1 CARTON / 30 mL in 1 BOTTLE, GLASS (64141-001-02)

Product Details

What is NDC 64141-001?

The NDC code 64141-001 is assigned by the FDA to the product Bobbi Brown Skin Foundation Spf 15 which is product labeled by Bobbi Brown Professional Cosmetics Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64141-001-01 1 bottle, glass in 1 carton / 30 ml in 1 bottle, glass (64141-001-02). 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 Bobbi Brown Skin Foundation Spf 15?

This product is used as INDICATIONS: PROVIDES BROAD SPECTRUM PROTECTION FROM SUN'S DAMAGING RAYS.USAGE: SHAKE WELL BEFORE USE. APPLY PRIOR TO SUN EXPOSURE

Which are Bobbi Brown Skin Foundation Spf 15 UNII Codes?

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

* Please review the disclaimer below.

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".