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NDC 10096-0149 Anew Rejuvenate 24 Hour Eye Moisturizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10096-0149?
  4. Anew Rejuvenate 24 Hour Eye Moisturizer Uses
  5. Active 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:
10096-0149
Proprietary Name:
Anew Rejuvenate 24 Hour Eye Moisturizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avon Products, Inc
Labeler Code:
10096
Product Label ID:
85f54074-5fd2-42a4-8f83-92a3ed0ca251
Start Marketing Date: [9]
02-08-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 10096-0149?

The NDC code 10096-0149 is assigned by the FDA to the product Anew Rejuvenate 24 Hour Eye Moisturizer which is product labeled by Avon Products, Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10096-0149-2 1 jar in 1 carton / 10 ml in 1 jar (10096-0149-1), 10096-0149-3 1.1 ml in 1 packet . 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 Anew Rejuvenate 24 Hour Eye Moisturizer?

This product is used as Purpose................................Sunscreen

Which are Anew Rejuvenate 24 Hour Eye Moisturizer UNII Codes?

The UNII codes for the active 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".