NDC 69038-040 Burberry Cashmere Long-lasting Flawless Soft-matte Foundation Sunscreen Spf20 Porcelain

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:
69038-040
Proprietary Name:
Burberry Cashmere Long-lasting Flawless Soft-matte Foundation Sunscreen Spf20 Porcelain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Burberry Limited
Labeler Code:
69038
Start Marketing Date: [9]
11-06-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69038-040-30

Package Description: 1 PACKAGE in 1 PACKAGE / 30 mL in 1 PACKAGE

Product Details

What is NDC 69038-040?

The NDC code 69038-040 is assigned by the FDA to the product Burberry Cashmere Long-lasting Flawless Soft-matte Foundation Sunscreen Spf20 Porcelain which is product labeled by Burberry Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69038-040-30 1 package in 1 package / 30 ml in 1 package. 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 Burberry Cashmere Long-lasting Flawless Soft-matte Foundation Sunscreen Spf20 Porcelain?

Reapp ly at least every 2 hrs. Use a water resistant sunscreen if swimming or sweating.Apply liberal ly 15 mins before sun exposure. Children under 6 months of age: Ask a doctor.

Which are Burberry Cashmere Long-lasting Flawless Soft-matte Foundation Sunscreen Spf20 Porcelain UNII Codes?

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

Which are Burberry Cashmere Long-lasting Flawless Soft-matte Foundation Sunscreen Spf20 Porcelain 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".