NDC 77731-105 Purelogic 100ct Lemon Antibacterial Wipe Canister

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
77731-105
Proprietary Name:
Purelogic 100ct Lemon Antibacterial Wipe Canister
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Argento Sc By Sicura Inc.
Labeler Code:
77731
Start Marketing Date: [9]
05-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 77731-105-01

Package Description: 100 CLOTH in 1 BAG

Product Details

What is NDC 77731-105?

The NDC code 77731-105 is assigned by the FDA to the product Purelogic 100ct Lemon Antibacterial Wipe Canister 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 77731-105-01 100 cloth in 1 bag . 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 100ct Lemon Antibacterial Wipe Canister?

Wipe product on hands thoroughly & allow to dry, do not wipe off.For children under 6, Use only with adult supervision.Not recommended for use with infants.

Which are Purelogic 100ct Lemon Antibacterial Wipe Canister UNII Codes?

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

Which are Purelogic 100ct Lemon Antibacterial Wipe Canister 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".