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  4. NDC Product Code: 76277-613 Ocumend Healing Gels

NDC 76277-613 Ocumend Healing Gels

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76277-613?
  4. Ocumend Healing Gels 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:
76277-613
Proprietary Name:
Ocumend Healing Gels
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cearna, Inc.
Labeler Code:
76277
Product Label ID:
2e05eba5-fd08-4d7f-e054-00144ff88e88
Start Marketing Date: [9]
03-11-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76277-613-21

Package Description: 13 POUCH in 1 CARTON / 2 PATCH in 1 POUCH

Product Details

What is NDC 76277-613?

The NDC code 76277-613 is assigned by the FDA to the product Ocumend Healing Gels which is product labeled by Cearna, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76277-613-21 13 pouch in 1 carton / 2 patch in 1 pouch. 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 Ocumend Healing Gels?

Use as directed by a physician. Place healing gels on intact skin and replace as needed.

Which are Ocumend Healing Gels UNII Codes?

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

Which are Ocumend Healing Gels 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:

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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".