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  4. NDC Product Code: 74743-007 Foaming Hand Wash

NDC 74743-007 Foaming Hand Wash

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74743-007?
  4. Foaming Hand Wash 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.
NDC Product Code:
74743-007
Proprietary Name:
Foaming Hand Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guangzhou Joy Claire Biological Technology Co., Ltd
Labeler Code:
74743
Product Label ID:
a3b7b24a-9593-d268-e053-2995a90a04ff
Start Marketing Date: [9]
04-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 74743-007?

The NDC code 74743-007 is assigned by the FDA to the product Foaming Hand Wash which is product labeled by Guangzhou Joy Claire Biological Technology Co., Ltd. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 74743-007-01 500 g in 1 bottle , 74743-007-02 400 g in 1 bottle , 74743-007-03 300 g in 1 bottle , 74743-007-04 250 g in 1 bottle , 74743-007-05 100 g in 1 bottle , 74743-007-06 60 g in 1 bottle , 74743-007-07 50 g in 1 bottle , 74743-007-08 30 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 Foaming Hand Wash?

Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rinse with clean active

Which are Foaming Hand Wash UNII Codes?

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

Which are Foaming 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".