NDC 58665-001 Freshnails The Undernail Sanitizer

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:
58665-001
Proprietary Name:
Freshnails The Undernail Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
58665
Start Marketing Date: [9]
11-19-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)

Code Structure Chart

Product Details

What is NDC 58665-001?

The NDC code 58665-001 is assigned by the FDA to the product Freshnails The Undernail Sanitizer which is product labeled by Twb Strategic Investments Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58665-001-02 1 bottle, with applicator in 1 carton / 5.75 ml in 1 bottle, with applicator. 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 Freshnails The Undernail Sanitizer?

Use For antiseptic hand cleaning to kill and decrease germs and bacteria on the skin, particularly on the fingertip and under the fingernail area. For personal hand hygiene and recommended for repeated use.Dries in seconds.

Which are Freshnails The Undernail Sanitizer UNII Codes?

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

Which are Freshnails The Undernail Sanitizer 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:

What is the NDC to RxNorm Crosswalk for Freshnails The Undernail Sanitizer?

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".