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  4. NDC Product Code: 72642-020 Dr Cosign Cce Premium Repair

NDC 72642-020 Dr Cosign Cce Premium Repair

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72642-020?
  4. Dr Cosign Cce Premium Repair 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:
72642-020
Proprietary Name:
Dr Cosign Cce Premium Repair
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Naerok Resources Co., Ltd
Labeler Code:
72642
Product Label ID:
460234aa-11d7-4889-92f9-c730144f6fee
Start Marketing Date: [9]
10-01-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 72642-020?

The NDC code 72642-020 is assigned by the FDA to the product Dr Cosign Cce Premium Repair which is product labeled by Naerok Resources Co., Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 72642-020-02 1 container in 1 carton / 50 ml in 1 container (72642-020-01), 72642-020-03 20 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 Dr Cosign Cce Premium Repair?

Directions:Apply an appropriate amount and gently tap for absorption, after evenly spreading over the face, in each end step morning, evening skin care.

Which are Dr Cosign Cce Premium Repair UNII Codes?

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

Which are Dr Cosign Cce Premium Repair 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".