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  4. NDC Product Code: 44672-112 Perisol Hand Sanitizer Foam

NDC 44672-112 Perisol Hand Sanitizer Foam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44672-112?
  4. Perisol Hand Sanitizer 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:
44672-112
Proprietary Name:
Perisol Hand Sanitizer Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pelican Group Llc, The
Labeler Code:
44672
Product Label ID:
bd36ff51-cc1e-10b5-e053-2995a90ae50a
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 44672-112-11

Package Description: 473.2 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 44672-112?

The NDC code 44672-112 is assigned by the FDA to the product Perisol Hand Sanitizer Foam which is product labeled by Pelican Group Llc, The. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44672-112-11 473.2 ml in 1 bottle, pump . 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 Perisol Hand Sanitizer Foam?

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry.Children under 6 years of age should be supervised when using this product.

Which are Perisol Hand Sanitizer Foam UNII Codes?

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

Which are Perisol Hand Sanitizer 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:

* 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".