NDC 51523-370 15hr Cover Lasting M201 Medium Beige Spf50

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:
51523-370
Proprietary Name:
15hr Cover Lasting M201 Medium Beige Spf50
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Thefaceshop Co., Ltd.
Labeler Code:
51523
Start Marketing Date: [9]
10-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51523-370-22

Package Description: 1 TUBE in 1 CARTON / 35 g in 1 TUBE

Product Details

What is NDC 51523-370?

The NDC code 51523-370 is assigned by the FDA to the product 15hr Cover Lasting M201 Medium Beige Spf50 which is product labeled by Thefaceshop Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51523-370-22 1 tube in 1 carton / 35 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 15hr Cover Lasting M201 Medium Beige Spf50?

Apply generously and evenly 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor. Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. Dispense an adequate amount and apply to skin. Pat skin lightly to boost absorption.

Which are 15hr Cover Lasting M201 Medium Beige Spf50 UNII Codes?

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

Which are 15hr Cover Lasting M201 Medium Beige Spf50 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".