NDC 64709-101 Diamond Wipes Antibacterial Hand Wipes

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:
64709-101
Proprietary Name:
Diamond Wipes Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Diamond Wipes International, Inc.
Labeler Code:
64709
Start Marketing Date: [9]
01-01-2010
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 64709-101-10

Package Description: 1.8 mL in 1 PACKET

Product Details

What is NDC 64709-101?

The NDC code 64709-101 is assigned by the FDA to the product Diamond Wipes Antibacterial Hand Wipes which is product labeled by Diamond Wipes International, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64709-101-10 1.8 ml 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 Diamond Wipes Antibacterial Hand Wipes?

For hand washing to decrease bacteria on skinreccomended for repeated use open packetremove and unfold wipeswipe hands thoroughly for approximately 15 secondsdo not flush

Which are Diamond Wipes Antibacterial Hand Wipes UNII Codes?

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

Which are Diamond Wipes Antibacterial Hand Wipes 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".