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  4. NDC Product Code: 77731-053 Purelogic Foaming Hand Sanitizer Lemon Mint

NDC 77731-053 Purelogic Foaming Hand Sanitizer Lemon Mint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77731-053?
  4. Purelogic Foaming Hand Sanitizer Lemon Mint 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:
77731-053
Proprietary Name:
Purelogic Foaming Hand Sanitizer Lemon Mint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Argento Sc By Sicura Inc.
Labeler Code:
77731
Product Label ID:
7472b2b7-e16e-4d23-a7d1-bf86f465ff32
Start Marketing Date: [9]
07-31-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77731-053-01

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 77731-053?

The NDC code 77731-053 is assigned by the FDA to the product Purelogic Foaming Hand Sanitizer Lemon Mint which is product labeled by Argento Sc By Sicura Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77731-053-01 500 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 Purelogic Foaming Hand Sanitizer Lemon Mint?

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

Which are Purelogic Foaming Hand Sanitizer Lemon Mint UNII Codes?

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

Which are Purelogic Foaming Hand Sanitizer Lemon Mint 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 Purelogic Foaming Hand Sanitizer Lemon Mint?

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".