NDC 50125-001 Medessence Plus Homeopathic Nail

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:
50125-001
Proprietary Name:
Medessence Plus Homeopathic Nail
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Deep Cover Systems Llc
Labeler Code:
50125
Start Marketing Date: [9]
05-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50125-001-10

Package Description: 10 mL in 1 PACKET

Product Details

What is NDC 50125-001?

The NDC code 50125-001 is assigned by the FDA to the product Medessence Plus Homeopathic Nail which is product labeled by Deep Cover Systems Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50125-001-10 10 ml in 1 packet . 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 Medessence Plus Homeopathic Nail?

For Directions, uses and other information:See the package insert

Which are Medessence Plus Homeopathic Nail UNII Codes?

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

* Please review the disclaimer below.

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".