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NDC 73560-0004 Youllief Perfect Balanced Sun Skincare

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73560-0004?
  4. Youllief Perfect Balanced Sun Skincare 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:
73560-0004
Proprietary Name:
Youllief Perfect Balanced Sun Skincare
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Plcoskin
Labeler Code:
73560
Product Label ID:
9d2caaac-44f1-598f-e053-2995a90ad7f4
Start Marketing Date: [9]
01-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73560-0004-1

Package Description: 60 mL in 1 TUBE

Product Details

What is NDC 73560-0004?

The NDC code 73560-0004 is assigned by the FDA to the product Youllief Perfect Balanced Sun Skincare which is product labeled by Plcoskin. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73560-0004-1 60 ml in 1 tube . 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 Youllief Perfect Balanced Sun Skincare?

Every morning and evening, after the usage of ampoules or essences, take a moderate amount of the cosmetics and softly spread along the eye area and parts where wrinkles are considerates then gently pat for the skin to absorb.

Which are Youllief Perfect Balanced Sun Skincare UNII Codes?

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

Which are Youllief Perfect Balanced Sun Skincare 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".