1. Home
  2. Labeler Index
  3. Thefaceshop Co., Ltd.
  4. NDC Product Code: 51523-020 Natural Sun Aq Power Long Lasting Sun Spf45 Pa

NDC 51523-020 Natural Sun Aq Power Long Lasting Sun Spf45 Pa

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51523-020?
  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:
51523-020
Proprietary Name:
Natural Sun Aq Power Long Lasting Sun Spf45 Pa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Thefaceshop Co., Ltd.
Labeler Code:
51523
Product Label ID:
41e058ac-2230-4047-8f6e-3054167a881b
Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51523-020-01

Package Description: 50 mL in 1 CARTON

Product Details

What is NDC 51523-020?

The NDC code 51523-020 is assigned by the FDA to the product Natural Sun Aq Power Long Lasting Sun Spf45 Pa 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 51523-020-01 50 ml 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 Natural Sun Aq Power Long Lasting Sun Spf45 Pa 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".