1. Home
  2. Labeler Index
  3. Kantian Skincare, Llc
  4. NDC Product Code: 57524-013 Ephiderm Spot Treatment

NDC 57524-013 Ephiderm Spot Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57524-013?
  4. Ephiderm Spot Treatment Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
57524-013
Proprietary Name:
Ephiderm Spot Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kantian Skincare, Llc
Labeler Code:
57524
Product Label ID:
1c31c336-d659-4865-9515-25b9f387edbc
Start Marketing Date: [9]
01-10-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57524-013?

The NDC code 57524-013 is assigned by the FDA to the product Ephiderm Spot Treatment which is product labeled by Kantian Skincare, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57524-013-01 28 g in 1 tube . 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 Ephiderm Spot Treatment?

Apply a thin layer to the affected area, In the morning and evening. For best results, apply epHiderm Synergyzer after epHiderm Spot Treatment. Wash hands thoroughly after application.

Which are Ephiderm Spot Treatment UNII Codes?

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

Which are Ephiderm Spot Treatment 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:

* 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".