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  4. NDC Product Code: 54796-001 Antibacterial Foam Hand Wash

NDC 54796-001 Antibacterial Foam Hand Wash

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54796-001?
  5. Antibacterial Foam Hand Wash 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:
54796-001
Proprietary Name:
Antibacterial Foam Hand Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wuxi Youjie Technology Co. Ltd
Labeler Code:
54796
Product Label ID:
a456a006-3cb1-0c13-e053-2995a90ab8f2
Start Marketing Date: [9]
04-28-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Imprint(s):
ECOFINEST

Code Structure Chart

Product Details

What is NDC 54796-001?

The NDC code 54796-001 is assigned by the FDA to the product Antibacterial Foam Hand Wash which is product labeled by Wuxi Youjie Technology Co. Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54796-001-01 450 g in 1 bottle . 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 Foam Hand Wash?

After wetting your hands, put a proper amount of liquid soap in your hands, gently rub them for 2 minutes, and then rinse them with water.

Which are Antibacterial Foam Hand Wash UNII Codes?

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

Which are Antibacterial Foam Hand Wash 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".