NDC 67938-1436 Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11

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:
67938-1436
Proprietary Name:
Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Elizabeth Arden, Inc
Labeler Code:
67938
Start Marketing Date: [9]
09-20-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328 - PURE FINISH 11)

Product Packages

NDC Code 67938-1436-1

Package Description: 1 CONTAINER in 1 BOX / 8.33 g in 1 CONTAINER (67938-1436-2)

Product Details

What is NDC 67938-1436?

The NDC code 67938-1436 is assigned by the FDA to the product Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11 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 67938-1436-1 1 container in 1 box / 8.33 g in 1 container (67938-1436-2). 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 Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11?

To Use: Turn dial to the right to release product. Smooth on to face before sun exposure.

Which are Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11 UNII Codes?

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

Which are Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11 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".