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  4. NDC Product Code: 51523-009 Flebeaute Collagenic Two Way Cake Spf17 Pa Nb21

NDC 51523-009 Flebeaute Collagenic Two Way Cake Spf17 Pa Nb21

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51523-009?
  4. 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:
51523-009
Proprietary Name:
Flebeaute Collagenic Two Way Cake Spf17 Pa Nb21
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Thefaceshop Co., Ltd.
Labeler Code:
51523
Product Label ID:
582f1761-76c0-435d-80d5-0cbff289f649
Start Marketing Date: [9]
07-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51523-009-01

Package Description: 12 g in 1 CARTON

Product Details

What is NDC 51523-009?

The NDC code 51523-009 is assigned by the FDA to the product Flebeaute Collagenic Two Way Cake Spf17 Pa Nb21 which is product labeled by Thefaceshop Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51523-009-01 12 g in 1 carton . 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.

Which are Flebeaute Collagenic Two Way Cake Spf17 Pa Nb21 UNII Codes?

The UNII codes for the active 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".