NDC 52424-0001 Bio Beauty Bio Defense Tinted Foundation Spf 18

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52424-0001
Proprietary Name:
Bio Beauty Bio Defense Tinted Foundation Spf 18
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Libinvest
Labeler Code:
52424
Start Marketing Date: [9]
06-20-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52424-0001-0

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 50 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 52424-0001?

The NDC code 52424-0001 is assigned by the FDA to the product Bio Beauty Bio Defense Tinted Foundation Spf 18 which is product labeled by Libinvest. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52424-0001-0 1 bottle, plastic in 1 box / 50 ml in 1 bottle, plastic. 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 Bio Beauty Bio Defense Tinted Foundation Spf 18?

Use in place of your normal foundation.

Which are Bio Beauty Bio Defense Tinted Foundation Spf 18 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".