NDC 43596-0020 Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Obscure 10

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:
43596-0020
Proprietary Name:
Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Obscure 10
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ventura Corporation, Ltd
Labeler Code:
43596
Start Marketing Date: [9]
03-24-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43596-0020-0

Package Description: 8 g in 1 JAR

Product Details

What is NDC 43596-0020?

The NDC code 43596-0020 is assigned by the FDA to the product Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Obscure 10 which is product labeled by Ventura Corporation, Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43596-0020-0 8 g in 1 jar . 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 Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Obscure 10?

Apply liberally and evenly 15 minutes before sun exposure. Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating. Children under 6 months of age: Ask a doctor.

Which are Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Obscure 10 UNII Codes?

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

Which are Lbel Effet Parfait Spots Reducing Effect Foundation Spf 18 - Obscure 10 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".