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  4. NDC Product Code: 43333-454 Antibacterial Foaming Hand Wash Sweet Treats

NDC 43333-454 Antibacterial Foaming Hand Wash Sweet Treats

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43333-454?
  4. Antibacterial Foaming Hand Wash Sweet Treats 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:
43333-454
Proprietary Name:
Antibacterial Foaming Hand Wash Sweet Treats
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tonic Bath And Body Products Shenzhen Ltd.
Labeler Code:
43333
Product Label ID:
1d254a4f-6ed2-447f-bd16-8592e48ed170
Start Marketing Date: [9]
06-25-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43333-454-16

Package Description: 500 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 43333-454?

The NDC code 43333-454 is assigned by the FDA to the product Antibacterial Foaming Hand Wash Sweet Treats which is product labeled by Tonic Bath And Body Products Shenzhen Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43333-454-16 500 ml in 1 bottle, pump . 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 Foaming Hand Wash Sweet Treats?

Wet hands. Apply palmful to hands and forearms. Scrub thoroughly. Rinse and repeat. Dry thoroughly.

Which are Antibacterial Foaming Hand Wash Sweet Treats UNII Codes?

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

Which are Antibacterial Foaming Hand Wash Sweet Treats 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".