62742-4032 NDC - LYCOGEL COVER AND RECOVERY - BREATHABLE CONCEALER - SPF 30 WITH LYCO COMPLEX (TITANIUM DIOXIDE AND ZINC OXIDE)

Drug Information

Product NDC: 62742-4032

Proprietary Name: Lycogel Cover and Recovery - Breathable Concealer - SPF 30 with LYCO Complex

Non Proprietary Name: Titanium Dioxide and Zinc Oxide

Active Ingredient(s):
  • 65 mg/mL TITANIUM DIOXIDE;
  • 82 mg/mL ZINC OXIDE


Administration Route(s): TOPICAL

Dosage Form(s): CREAM

Labeler Information

Labeler Name: Allure Cosmetic, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:2/1/2010

Package Information

No. Package Code Package Description Billing Unit
162742-4032-21 TUBE in 1 CARTON (62742-4032-2) > 6 mL in 1 TUBE (62742-4032-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62742-4032The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELycogel Cover and Recovery - Breathable Concealer - SPF 30 with LYCO ComplexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMETitanium Dioxide and Zinc OxideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEAllure Cosmetic, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMETITANIUM DIOXIDE; ZINC OXIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH65; 82 
ACTIVE INGRED UNITmg/mL; mg/mL 

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This page was last updated on: 9/13/2019