NDC 52738-005 Jisberry Antibacterial Handlotion

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:
52738-005
Proprietary Name:
Jisberry Antibacterial Handlotion
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
52738
Start Marketing Date: [9]
04-12-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 52738-005?

The NDC code 52738-005 is assigned by the FDA to the product Jisberry Antibacterial Handlotion which is product labeled by Hangzhou Xizi Sanitary Disinfection Medical Equipment Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52738-005-01 500 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 Jisberry Antibacterial Handlotion?

1.Hand washing before surgery: Wet hands with flowing water first, then apply a proper amount of liquid into hands, wash hands, forearms and lower 1/3 of upper arm according to the requirements of hand hygiene standards, rub thoroughly for 2 minutes and rinse with flowing water. 2.Sanitary hand washing: Wet hands with flowing water first, then apply a proper amount of liquid into hands, rub evenly and thoroughly for 2 minutes according to the requirements of hand hygiene standards, and rinse with flowing water.

Which are Jisberry Antibacterial Handlotion UNII Codes?

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

Which are Jisberry Antibacterial Handlotion 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".