NDC 62742-4045 Clear Cell Cleanser

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:
62742-4045
Proprietary Name:
Clear Cell Cleanser
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 62742-4045-1

Package Description: 177.6 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 62742-4045?

The NDC code 62742-4045 is assigned by the FDA to the product Clear Cell Cleanser 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 62742-4045-1 177.6 ml in 1 bottle, plastic . 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 Clear Cell Cleanser?

INDICATIONS AND USAGE SECTION:A daily Salicylic acid cleanser that exfoiates, gently removes makeup and diminishes excess oil. Anti-oxidants keep skin soft, purified and shine-free.Paraben freeDIRECTIONS:Apply to wet face and massage for 1 minute. Repeat cleansing for additional exfoliation.INDICATIONS:Acne and acne-prone skin

Which are Clear Cell Cleanser UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Clear Cell Cleanser?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".