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  4. NDC Product Code: 50795-1001 U-max Wrinkle Serum

NDC 50795-1001 U-max Wrinkle Serum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50795-1001?
  4. U-max Wrinkle Serum 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:
50795-1001
Proprietary Name:
U-max Wrinkle Serum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vs Shinbi Co., Ltd.
Labeler Code:
50795
Product Label ID:
54f4e0e8-7ee2-4f27-923e-c6db705a53c7
Start Marketing Date: [9]
06-04-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50795-1001-1

Package Description: 50 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 50795-1001?

The NDC code 50795-1001 is assigned by the FDA to the product U-max Wrinkle Serum which is product labeled by Vs Shinbi Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50795-1001-1 50 ml in 1 bottle, with applicator . 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 U-max Wrinkle Serum?

- apply only for skin- apply 2 or 3 times a day with 5~6ml- massage with your finger over 2 min and let them dry

Which are U-max Wrinkle Serum UNII Codes?

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

Which are U-max Wrinkle Serum 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".