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NDC 69225-1000 Antiseptic Bandages

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69225-1000?
  4. Antiseptic Bandages Uses
  5. Active 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:
69225-1000
Proprietary Name:
Antiseptic Bandages
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmaband
Labeler Code:
69225
Product Label ID:
b5a44e5f-c84a-40e2-831b-08925d7ef97e
Start Marketing Date: [9]
01-09-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69225-1000-2

Package Description: 20 DRESSING in 1 BOX

NDC Code 69225-1000-3

Package Description: 30 DRESSING in 1 BOX

NDC Code 69225-1000-4

Package Description: 40 DRESSING in 1 BOX

Product Details

What is NDC 69225-1000?

The NDC code 69225-1000 is assigned by the FDA to the product Antiseptic Bandages which is product labeled by Pharmaband. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 69225-1000-2 20 dressing in 1 box , 69225-1000-3 30 dressing in 1 box , 69225-1000-4 40 dressing in 1 box . 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 Antiseptic Bandages?

Clean and dry the affected area. Apply a sterile bandage on the area 1 to 3 times daily.

Which are Antiseptic Bandages UNII Codes?

The UNII codes for the active 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".