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  4. NDC Product Code: 77731-011 Purelogic Antibacterial Wipes Refreshing Aloe

NDC 77731-011 Purelogic Antibacterial Wipes Refreshing Aloe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77731-011?
  4. Purelogic Antibacterial Wipes Refreshing Aloe 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:
77731-011
Proprietary Name:
Purelogic Antibacterial Wipes Refreshing Aloe
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:
341b180b-8f75-429d-bda8-f79652b4163f
Start Marketing Date: [9]
07-23-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77731-011-01

Package Description: 85 SOLUTION in 1 CANISTER

Product Details

What is NDC 77731-011?

The NDC code 77731-011 is assigned by the FDA to the product Purelogic Antibacterial Wipes Refreshing Aloe 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 77731-011-01 85 solution in 1 canister . 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 Antibacterial Wipes Refreshing Aloe?

Wipe product on hands thoroughly and allow to dry, do not wipe offFor children under 6, use under adult supervisionNot recommended for use with infants

Which are Purelogic Antibacterial Wipes Refreshing Aloe UNII Codes?

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

Which are Purelogic Antibacterial Wipes Refreshing Aloe 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".