Devolver Disinfecting Wipes
NDC 75001-206

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 75001-206?
  4. Devolver Disinfecting 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.

Devolver Disinfecting Wipes is a UNAPPROVED DRUG OTHER-approved product labeled by Devolver Cosmetics Co., Ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 75001-206 and 5 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
75001-206
Proprietary Name:
Devolver Disinfecting Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Devolver Cosmetics Co., Ltd
Labeler Code:
75001
Product Label ID:
b11ebbc4-6b6f-1540-e053-2a95a90aad42
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
10-08-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 75001-206?

The NDC code 75001-206 is assigned by the FDA to the product Devolver Disinfecting Wipes. This pharmaceutical product is labeled by Devolver Cosmetics Co., Ltd and is currently categorized as listed product. In terms of distribution, this product is available in 5 different package configurations. The associated package NDC(s) include: 75001-206-01, 75001-206-02, 75001-206-03, 75001-206-04, 75001-206-05. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

1. Before first use : Remove cap and seal. Take the corner of the center sheet and thread it through the dispensing flap of the container cap. Replace cap.2. Open container and tear off sheet.3. Erase all dry-erase markings from surface to be cleaned.4. Wipe surface thoroughly and discard towelette.5. Keep the container cap closed after each use. * Cleans and restores dry-erase surfaces* Use Dry-Erase Board Cleaning Wipes to remove dry-erase marker shadows, ghosting and stains* Safe, Low Odor, Non-Toxic and Flame Resistant* Hands stay clean* Safe to use on most surfaces

Which are the associated UNII Codes?

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

  • N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)
  • N-ALKYL DIMETHYL BENZYL AMMONIUM ION (C12-C18) (UNII: 3QBE2Z8KR2) (Active Moiety)

Which are the Inactive Ingredients associated 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 full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".