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  4. NDC Product Code: 72306-001 Allseason Antibacterial Bandage

NDC 72306-001 Allseason Antibacterial Bandage

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72306-001?
  4. Allseason Antibacterial Bandage 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:
72306-001
Proprietary Name:
Allseason Antibacterial Bandage
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Excellence Medical Supplies Co., Ltd.
Labeler Code:
72306
Product Label ID:
181244e6-416f-498e-a9f2-4066b2e051d8
Start Marketing Date: [9]
06-05-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72306-001-01

Package Description: 30 POUCH in 1 PACKAGE / 3.125 cm2 in 1 POUCH

Product Details

What is NDC 72306-001?

The NDC code 72306-001 is assigned by the FDA to the product Allseason Antibacterial Bandage which is product labeled by Excellence Medical Supplies Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72306-001-01 30 pouch in 1 package / 3.125 cm2 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 Allseason Antibacterial Bandage?

UsesFor use in minor cuts, scrapes and burns.Proper care is important to avoid infections or future complications.

Which are Allseason Antibacterial Bandage UNII Codes?

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

Which are Allseason Antibacterial Bandage 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".