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  4. NDC Product Code: 52738-003 Jisberry Disposabie Quick-drying Hand Sanitizing

NDC 52738-003 Jisberry Disposabie Quick-drying Hand Sanitizing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52738-003?
  5. Jisberry Disposabie Quick-drying Hand Sanitizing Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52738-003
Proprietary Name:
Jisberry Disposabie Quick-drying Hand Sanitizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Xizi Sanitary Disinfection Medical Equipment Co., Ltd
Labeler Code:
52738
Product Label ID:
a33cda34-3263-546e-e053-2995a90ab1f9
Start Marketing Date: [9]
04-14-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Size(s):
150 MM

Product Packages

NDC Code 52738-003-01

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 52738-003?

The NDC code 52738-003 is assigned by the FDA to the product Jisberry Disposabie Quick-drying Hand Sanitizing 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 52738-003-01 500 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 Jisberry Disposabie Quick-drying Hand Sanitizing?

1. Surgical hand disinfection: wash hands,forearms and 1/3 of the lower part of the upper arm according to the requirements of hand hygiene specifications, and then take a proper amount of Jisberry and rub it to each part of the hands, forearms and 1/3 of the lower part of the upper arm for 1-3 minutes.2. Hand sanitization: apply proper amount of Jisberry to the palm,knead according to the requirements of hand sanitization specification until the liquid completely covers the skin of hand, and act for 1minute.3. Skin disinfection: apply appropriate amount of Jisberry to the skin of the area to be disinfected for 1 minute.

Which are Jisberry Disposabie Quick-drying Hand Sanitizing UNII Codes?

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

Which are Jisberry Disposabie Quick-drying Hand Sanitizing 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:

  • FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
  • CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
  • CUPRIC BIS(TRIETHANOLAMINE) (UNII: YBM44X0B6H)

What is the NDC to RxNorm Crosswalk for Jisberry Disposabie Quick-drying Hand Sanitizing?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".