NDC 10096-0257 Ideal Flawless Invisible Coverage Liquid Foundation

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10096-0257
Proprietary Name:
Ideal Flawless Invisible Coverage Liquid Foundation
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avon Products, Inc
Labeler Code:
10096
Start Marketing Date: [9]
04-08-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10096-0257-2

Package Description: 1 BOTTLE, PUMP in 1 CARTON / 30 mL in 1 BOTTLE, PUMP (10096-0257-1)

Product Details

What is NDC 10096-0257?

The NDC code 10096-0257 is assigned by the FDA to the product Ideal Flawless Invisible Coverage Liquid Foundation which is product labeled by Avon Products, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10096-0257-2 1 bottle, pump in 1 carton / 30 ml in 1 bottle, pump (10096-0257-1). 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 Ideal Flawless Invisible Coverage Liquid Foundation?

Uses• helps prevent sunburn

Which are Ideal Flawless Invisible Coverage Liquid Foundation UNII Codes?

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

* Please review the disclaimer below.

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".