NDC 54607-003 Antibacterial Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
54607-003
Proprietary Name:
Antibacterial Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wuxi Yongning Daily Chemical Factory
Labeler Code:
54607
Start Marketing Date: [9]
03-29-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Imprint(s):
SUAYI

Product Packages

NDC Code 54607-003-01

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 54607-003?

The NDC code 54607-003 is assigned by the FDA to the product Antibacterial Hand Sanitizer which is product labeled by Wuxi Yongning Daily Chemical Factory. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54607-003-01 500 ml 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 Hand Sanitizer?

Rotate the pump head to the front exit, gently press the pump head, press out an appropriate amount of foam on both hands, and fully rub about 2 minutes, then wash with clean water.

Which are Antibacterial Hand Sanitizer UNII Codes?

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

  • 2-CHLORO-4,5-DIMETHYLPHENOL (UNII: 601F79M480)
  • 2-CHLORO-4,5-DIMETHYLPHENOL (UNII: 601F79M480) (Active Moiety)

Which are Antibacterial Hand Sanitizer 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".