NDC 62742-4041 Sun Tinted Solar Defense Organic Spf 30

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:
62742-4041
Proprietary Name:
Sun Tinted Solar Defense Organic Spf 30
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 62742-4041-1

Package Description: 56.7 mL in 1 TUBE

Product Details

What is NDC 62742-4041?

The NDC code 62742-4041 is assigned by the FDA to the product Sun Tinted Solar Defense Organic Spf 30 which is product labeled by Allure Labs, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62742-4041-1 56.7 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 Sun Tinted Solar Defense Organic Spf 30?

Directions:Apply liberally 15-30 minutes prior to sun exposure or as needed for a even skin tone. Reapply regulary or after prolonged swimming or activity.Indications:Sensitive skin, Sun exposure, uneven skin tone

Which are Sun Tinted Solar Defense Organic Spf 30 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".