NDC 77731-021 Purelogic Antibacterial Hand Wipes Lemon Mint 8 Travel Packs

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:
77731-021
Proprietary Name:
Purelogic Antibacterial Hand Wipes Lemon Mint 8 Travel Packs
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
77731
FDA Application Number: [6]
part333A
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date: [9]
07-24-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 77731-021?

The NDC code 77731-021 is assigned by the FDA to the product Purelogic Antibacterial Hand Wipes Lemon Mint 8 Travel Packs 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 77731-021-01 8 packet in 1 box / 20 solution in 1 packet. 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 Hand Wipes Lemon Mint 8 Travel Packs?

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 Hand Wipes Lemon Mint 8 Travel Packs UNII Codes?

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

Which are Purelogic Antibacterial Hand Wipes Lemon Mint 8 Travel Packs 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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".