NDC 67938-2008 Flawless Finish Perfectly Nude Makeup Broad Spectrum Sunscreen Spf 15 Shade Cream Nude

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:
67938-2008
Proprietary Name:
Flawless Finish Perfectly Nude Makeup Broad Spectrum Sunscreen Spf 15 Shade Cream Nude
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Elizabeth Arden, Inc
Labeler Code:
67938
Start Marketing Date: [9]
07-17-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - LIGHT BEIGE)

Product Packages

NDC Code 67938-2008-1

Package Description: 1 BOTTLE in 1 BOX / 1500 mg in 1 BOTTLE (67938-2008-2)

Product Details

What is NDC 67938-2008?

The NDC code 67938-2008 is assigned by the FDA to the product Flawless Finish Perfectly Nude Makeup Broad Spectrum Sunscreen Spf 15 Shade Cream Nude which is product labeled by Elizabeth Arden, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67938-2008-1 1 bottle in 1 box / 1500 mg in 1 bottle (67938-2008-2). 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 Flawless Finish Perfectly Nude Makeup Broad Spectrum Sunscreen Spf 15 Shade Cream Nude?

Smooth onto face.

Which are Flawless Finish Perfectly Nude Makeup Broad Spectrum Sunscreen Spf 15 Shade Cream Nude UNII Codes?

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

Which are Flawless Finish Perfectly Nude Makeup Broad Spectrum Sunscreen Spf 15 Shade Cream Nude 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:

* 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".