NDC 51386-724 Napoleon Perdis Sheer Genius Liquid Foundation Broad Spectrum Spf 20 Look 4

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:
51386-724
Proprietary Name:
Napoleon Perdis Sheer Genius Liquid Foundation Broad Spectrum Spf 20 Look 4
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Napoleon Perdis Cosmetics, Inc
Labeler Code:
51386
Start Marketing Date: [9]
12-12-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51386-724-00

Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE

Product Details

What is NDC 51386-724?

The NDC code 51386-724 is assigned by the FDA to the product Napoleon Perdis Sheer Genius Liquid Foundation Broad Spectrum Spf 20 Look 4 which is product labeled by Napoleon Perdis Cosmetics, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51386-724-00 1 tube in 1 carton / 30 ml in 1 tube. 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 Napoleon Perdis Sheer Genius Liquid Foundation Broad Spectrum Spf 20 Look 4?

Apply evenly before sun exposure. Children under 6 months of age: ask a doctor. Reapply as needed or after towel drying, swimming or sweating.

Which are Napoleon Perdis Sheer Genius Liquid Foundation Broad Spectrum Spf 20 Look 4 UNII Codes?

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

Which are Napoleon Perdis Sheer Genius Liquid Foundation Broad Spectrum Spf 20 Look 4 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".