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  4. NDC Product Code: 71146-0003 Peptide Volume Essence Premium

NDC 71146-0003 Peptide Volume Essence Premium

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71146-0003?
  4. Peptide Volume Essence Premium 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:
71146-0003
Proprietary Name:
Peptide Volume Essence Premium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
J&coceu Co Ltd
Labeler Code:
71146
Product Label ID:
5761d76b-7370-59fa-e053-2a91aa0aea53
Start Marketing Date: [9]
08-23-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 71146-0003?

The NDC code 71146-0003 is assigned by the FDA to the product Peptide Volume Essence Premium which is product labeled by J&coceu Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71146-0003-1 100 ml in 1 bottle, pump . 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 Peptide Volume Essence Premium?

After applying a generous, even layer to skin.If bubble up, Pat it lightly on your skin to absorb.

Which are Peptide Volume Essence Premium UNII Codes?

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

Which are Peptide Volume Essence Premium 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".