NDC 74212-1002 Disinfectant Wipes

Product Information

Disinfectant Wipes is product labeled by Accelerate360 Llc. The product's dosage form is and is administered via form.

Product Code74212-1002
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Disinfectant Wipes
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Accelerate360 Llc
Labeler Code74212
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
08-11-2020
Listing Expiration Date 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.
12-31-2021
Exclude Flag 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".
I
NDC Code Structure

What are the uses for Disinfectant Wipes?


Product Packages

NDC 74212-1002-1

Package Description: 10 PATCH in 1 BAG > 6 g in 1 PATCH

NDC 74212-1002-2

Package Description: 10 PATCH in 1 BAG > 6 g in 1 PATCH

NDC 74212-1002-3

Package Description: 50 PATCH in 1 BAG > 6 g in 1 PATCH

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

What are Disinfectant Wipes Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ALCOHOL (UNII: 3K9958V90M)
  • ALCOHOL (UNII: 3K9958V90M) (Active Moiety)

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

Inactive Ingredient(s)

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.
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
  • N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)

* Please review the disclaimer below.

Disinfectant Wipes Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



* Please review the disclaimer below.