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  4. NDC Product Code: 82131-325 Homworks Antibacterial Hand Wipes

NDC 82131-325 Homworks Antibacterial Hand Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82131-325?
  4. Homworks 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:
82131-325
Proprietary Name:
Homworks Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Acadian Crossing Consumer Products, Llc.
Labeler Code:
82131
Product Label ID:
c80e8d52-07bd-6454-e053-2a95a90a7279
Start Marketing Date: [9]
08-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82131-325?

The NDC code 82131-325 is assigned by the FDA to the product Homworks Antibacterial Hand Wipes which is product labeled by Acadian Crossing Consumer Products, Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82131-325-80 80 swab in 1 pouch . 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 Homworks Antibacterial Hand Wipes?

Directions: • Single use wipes for hands. • Close properly after dispensing to maintain purity, as alcohol by its nature evaporates quickly. • Dispose of properly. • DO NOT FLUSH. • Apply throughly to hands to cover all surfaces. • Rub hand together until dry.

Which are Homworks Antibacterial Hand Wipes UNII Codes?

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

Which are Homworks 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".