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  4. NDC Product Code: 71897-082 Unisource Peach Antimicrobial Foam

NDC 71897-082 Unisource Peach Antimicrobial Foam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71897-082?
  4. Unisource Peach Antimicrobial Foam 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:
71897-082
Proprietary Name:
Unisource Peach Antimicrobial Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Veritiv Operating Company
Labeler Code:
71897
Product Label ID:
8c365f23-50ea-498d-a226-7e26220ec208
Start Marketing Date: [9]
06-30-2006
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71897-082-40

Package Description: 1200 mL in 1 PACKAGE

Product Details

What is NDC 71897-082?

The NDC code 71897-082 is assigned by the FDA to the product Unisource Peach Antimicrobial Foam which is product labeled by Veritiv Operating Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71897-082-40 1200 ml in 1 package . 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 Unisource Peach Antimicrobial Foam?

Wet handsApply a small amount of product and work into a latherRinse well and dry hands completely

Which are Unisource Peach Antimicrobial Foam UNII Codes?

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

Which are Unisource Peach Antimicrobial Foam 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".