1. Home
  2. Labeler Index
  3. Aidance Skincare & Topical Solutions, Llc
  4. NDC Product Code: 24909-603 Fastrin Incontinence And Ostomy Rash Care

NDC 24909-603 Fastrin Incontinence And Ostomy Rash Care

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 24909-603?
  4. Fastrin Incontinence And Ostomy Rash Care 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:
24909-603
Proprietary Name:
Fastrin Incontinence And Ostomy Rash Care
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aidance Skincare & Topical Solutions, Llc
Labeler Code:
24909
Product Label ID:
3af07373-2bbc-4428-bb63-4313dc1dd8b5
Start Marketing Date: [9]
06-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 24909-603?

The NDC code 24909-603 is assigned by the FDA to the product Fastrin Incontinence And Ostomy Rash Care which is product labeled by Aidance Skincare & Topical Solutions, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 24909-603-10 10 g in 1 jar , 24909-603-50 50 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 Fastrin Incontinence And Ostomy Rash Care?

Clean and dry affected skin. Apply a thin layer of ointment over the affected area. Repeat 1 to 3 times daily or as needed.

Which are Fastrin Incontinence And Ostomy Rash Care UNII Codes?

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

Which are Fastrin Incontinence And Ostomy Rash Care 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".