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  4. NDC Product Code: 69082-700 Bac-d Foaming Antibacterial Wound Sanitizer

NDC 69082-700 Bac-d Foaming Antibacterial Wound Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69082-700?
  4. Bac-d Foaming Antibacterial Wound Sanitizer Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69082-700
Proprietary Name:
Bac-d Foaming Antibacterial Wound Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rdm Products, Inc
Labeler Code:
69082
Product Label ID:
146197f1-519b-4c55-9f91-f21b223c4d5d
Start Marketing Date: [9]
08-12-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69082-700-71

Package Description: 210 mL in 1 BOTTLE

Product Details

What is NDC 69082-700?

The NDC code 69082-700 is assigned by the FDA to the product Bac-d Foaming Antibacterial Wound Sanitizer which is product labeled by Rdm Products, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69082-700-71 210 ml in 1 bottle . 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 Bac-d Foaming Antibacterial Wound Sanitizer?

For ages two years and older. Pump a small amount on the area up to 3 times a day. Wipe off excess with sterile Gauze. Once dry, may be covered with a bandage  

Which are Bac-d Foaming Antibacterial Wound Sanitizer UNII Codes?

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

Which are Bac-d Foaming Antibacterial Wound Sanitizer 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:

What is the NDC to RxNorm Crosswalk for Bac-d Foaming Antibacterial Wound Sanitizer?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".