NDC 59958-240 Skinfuse Shield Spf 30

NDC Product Code 59958-240

NDC 59958-240-01

Package Description: 30 g in 1 TUBE

NDC 59958-240-02

Package Description: 60 g in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Skinfuse Shield Spf 30 with NDC 59958-240 is a product labeled by Owen Biosciences, Inc.. The generic name of Skinfuse Shield Spf 30 is . The product's dosage form is and is administered via form.

Labeler Name: Owen Biosciences, Inc.

Dosage Form: -

Product Type: What kind of product is this?
Indicates 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.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Owen Biosciences, Inc.
Labeler Code: 59958
Start Marketing Date: 11-17-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Skinfuse Shield Spf 30 Product Label Images