NDC 62742-4067 Prevention Daily Tinted Mositurizer Oil-free Tinted 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:
62742-4067
Proprietary Name:
Prevention Daily Tinted Mositurizer Oil-free Tinted 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
62742
Start Marketing Date: [9]
05-09-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62742-4067?

The NDC code 62742-4067 is assigned by the FDA to the product Prevention Daily Tinted Mositurizer Oil-free Tinted 30 which is product labeled by Allure Labs, Inc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 62742-4067-2 1 tube in 1 carton / 91 g in 1 tube (62742-4067-1), 62742-4067-3 170 g in 1 tube , 62742-4067-4 7 g 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 Prevention Daily Tinted Mositurizer Oil-free Tinted 30?

Uses:To help protect the skin from harmful UVA and UVB rays.If used as directed with other sun protection measures, this product reduces the risk of skin cancer and early skin aging, as well as helps prevent sunburn. DirectionsApply to cleansed skin every morning as daily moisturizer and for ultimate protectionRe-apply every 2 hours when exposed to sun or as needed

Which are Prevention Daily Tinted Mositurizer Oil-free Tinted 30 UNII Codes?

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

Which are Prevention Daily Tinted Mositurizer Oil-free Tinted 30 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".