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  4. NDC Product Code: 57718-110 Mizon Enjoy Vital Up Time Whitening Mask

NDC 57718-110 Mizon Enjoy Vital Up Time Whitening Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57718-110?
  4. Mizon Enjoy Vital Up Time Whitening Mask 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:
57718-110
Proprietary Name:
Mizon Enjoy Vital Up Time Whitening Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mizon Co., Ltd.
Labeler Code:
57718
Product Label ID:
b49fd4ed-2bd3-4611-9096-720151f2c752
Start Marketing Date: [9]
03-02-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 57718-110?

The NDC code 57718-110 is assigned by the FDA to the product Mizon Enjoy Vital Up Time Whitening Mask which is product labeled by Mizon Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57718-110-01 10 patch 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.

What are the uses for Mizon Enjoy Vital Up Time Whitening Mask?

Indications & Usage: 1. Use skin toner on cleansed face and take out the mask. 2. Place and attach mask on the face centered around the eyes. 3. Take off the mask after 10~20 minutes and pat the remaining essence until completely absorbed.

Which are Mizon Enjoy Vital Up Time Whitening Mask UNII Codes?

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

Which are Mizon Enjoy Vital Up Time Whitening Mask 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".