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  4. NDC Product Code: 74997-0012 W.skin White Glutathione Tone Up

NDC 74997-0012 W.skin White Glutathione Tone Up

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74997-0012?
  4. W.skin White Glutathione Tone Up 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:
74997-0012
Proprietary Name:
W.skin White Glutathione Tone Up
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
J&j Company
Labeler Code:
74997
Product Label ID:
c1c87c29-5bca-6526-e053-2a95a90a1cbd
Start Marketing Date: [9]
05-08-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74997-0012-1

Package Description: 60 mL in 1 TUBE

Product Details

What is NDC 74997-0012?

The NDC code 74997-0012 is assigned by the FDA to the product W.skin White Glutathione Tone Up which is product labeled by J&j Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 74997-0012-1 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 W.skin White Glutathione Tone Up?

Take an appropriate amount of this product and spread it evenly on the skin.Spread it out on neck if you feel your tone is not even with face.

Which are W.skin White Glutathione Tone Up UNII Codes?

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

Which are W.skin White Glutathione Tone Up 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".