1. Home
  2. Labeler Index
  3. Cosco International, Inc.
  4. NDC Product Code: 52261-0701 Forticept Antimicrobial Gel

NDC 52261-0701 Forticept Antimicrobial Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52261-0701?
  4. Forticept Antimicrobial Gel 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:
52261-0701
Proprietary Name:
Forticept Antimicrobial Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cosco International, Inc.
Labeler Code:
52261
Product Label ID:
9da1bd69-eab6-493b-8f5c-5247f8af237c
Start Marketing Date: [9]
10-27-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 52261-0701?

The NDC code 52261-0701 is assigned by the FDA to the product Forticept Antimicrobial Gel which is product labeled by Cosco International, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 52261-0701-0 60 g in 1 tube , 52261-0701-1 90 g in 1 tube , 52261-0701-2 120 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 Forticept Antimicrobial Gel?

Do not use on children under 2 years of age unless directed by a doctor.When using this product avoid contact with eyes.

Which are Forticept Antimicrobial Gel UNII Codes?

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

Which are Forticept Antimicrobial Gel 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".