NDC 62742-4052 Dermaquest Skin Therapy Solar Protection Spf 15

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:
62742-4052
Proprietary Name:
Dermaquest Skin Therapy Solar Protection Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allure Labs, Inc.
Labeler Code:
62742
Start Marketing Date: [9]
01-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62742-4052-1

Package Description: 29.6 mL in 1 TUBE

NDC Code 62742-4052-2

Package Description: 59.2 mL in 1 TUBE

Product Details

What is NDC 62742-4052?

The NDC code 62742-4052 is assigned by the FDA to the product Dermaquest Skin Therapy Solar Protection Spf 15 which is product labeled by Allure Labs, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 62742-4052-1 29.6 ml in 1 tube , 62742-4052-2 59.2 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 Dermaquest Skin Therapy Solar Protection Spf 15?

Optimal for daily use, this state-of-the-art, broad-spectrum sunscreen contains Zinc Oxide to help protect against the damaging effects of UVA and UVB rays. Cosmetically elegant and hydrating, this sunscreen id rapidly absorbed into the skin and is ideal for acne-prone akin and post-professional treatments.

Which are Dermaquest Skin Therapy Solar Protection Spf 15 UNII Codes?

The UNII codes for the active 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".