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  4. NDC Product Code: 74884-120 Antibacterial Hand Wipes

NDC 74884-120 Antibacterial Hand Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 74884-120?
  5. Antibacterial Hand Wipes Uses
  6. Active Ingredients UNII Codes
  7. 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:
74884-120
Proprietary Name:
Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
As Beauty
Labeler Code:
74884
Product Label ID:
a5f0cc00-a846-0aeb-e053-2995a90ae63b
Start Marketing Date: [9]
07-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Shape:
SQUARE (C48350)

Product Packages

NDC Code 74884-120-20

Package Description: 20 g in 1 POUCH

NDC Code 74884-120-60

Package Description: 60 g in 1 POUCH

Product Details

What is NDC 74884-120?

The NDC code 74884-120 is assigned by the FDA to the product Antibacterial Hand Wipes which is product labeled by As Beauty. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74884-120-20 20 g in 1 pouch , 74884-120-60 60 g 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 Antibacterial Hand Wipes?

Stop usage if a rash or irritation occurs.

Which are Antibacterial Hand Wipes UNII Codes?

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

Which are 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:

* 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".