68327-001 NDC - TOTAL COVER FX ()

Drug Information

  • Product NDC: 68327-001
  • Proprietary Name: Total Cover FX
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Cover FX Skin Care, Inc.
Product Type:
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:8/24/2012
End Marketing Date:5/5/2016

Package Information

No. Package Code Package Description Billing Unit
168327-001-0110 g in 1 CONTAINER (68327-001-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68327-001The 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.
PROPRIETARY NAMETotal Cover FXThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/24/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE5/5/2016Indicates 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.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBERpart352A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
LABELER NAMECover FX Skin Care, Inc.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

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This page was last updated on: 11/21/2025