NDC 92763-015 Disinfecting 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:
92763-015
Proprietary Name:
Disinfecting Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nanofixit Ventures Inc.
Labeler Code:
92763
Start Marketing Date: [9]
10-19-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 92763-015-01

Package Description: 50 CLOTH in 1 PACKET

Product Details

What is NDC 92763-015?

The NDC code 92763-015 is assigned by the FDA to the product Disinfecting Wipes which is product labeled by Nanofixit Ventures Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 92763-015-01 50 cloth 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 Disinfecting Wipes?

Thoroughly wipe the surface with the product and let it dry. Discardthe wipe properly. Supervise children under six years of age whenusing this product to avoid swallowing.

Which are Disinfecting Wipes UNII Codes?

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

  • N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)
  • N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14) (UNII: 85440928RV) (Active Moiety)
  • N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)
  • BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)

Which are Disinfecting 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".