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  4. NDC Product Code: 71928-7011 Wet Naps Antibacterial Hand Wipes

NDC 71928-7011 Wet Naps Antibacterial Hand Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71928-7011?
  4. Wet Naps Antibacterial Hand Wipes 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:
71928-7011
Proprietary Name:
Wet Naps Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Westrock Rkt Company
Labeler Code:
71928
Product Label ID:
60139664-3eb7-47fd-e053-2991aa0ad073
Start Marketing Date: [9]
01-01-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71928-7011-1

Package Description: 193 mL in 1 CANISTER

Product Details

What is NDC 71928-7011?

The NDC code 71928-7011 is assigned by the FDA to the product Wet Naps Antibacterial Hand Wipes which is product labeled by Westrock Rkt Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71928-7011-1 193 ml 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 Wet Naps Antibacterial Hand Wipes?

To dispense, life cover, remove seal, pull center sheet from toll, twist to point, feed through dispenser hole in cover. Keep lid closed to prevent moisture loss. Use as a part of your cleaning routine. Rub product onto hands and allow to dry. Discard after single use.

Which are Wet Naps Antibacterial Hand Wipes UNII Codes?

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

Which are Wet Naps 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:

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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".