NDC 53042-003 Luobenqing 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:
53042-003
Proprietary Name:
Luobenqing Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lustre Pharmaceutical Lab.co.,ltd.
Labeler Code:
53042
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Imprint(s):
LUOBENQING

Product Packages

NDC Code 53042-003-01

Package Description: 150 mL in 1 BOTTLE

Product Details

What is NDC 53042-003?

The NDC code 53042-003 is assigned by the FDA to the product Luobenqing Hand Sanitizer which is product labeled by Lustre Pharmaceutical Lab.co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53042-003-01 150 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 Luobenqing Hand Sanitizer?

Use appropriate amount on palm and rubbing few minutes.

Which are Luobenqing Hand Sanitizer UNII Codes?

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

Which are Luobenqing 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:

What is the NDC to RxNorm Crosswalk for Luobenqing Hand Sanitizer?

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:
  • RxCUI: 2286262 - ethanol 70 % / benzalkonium chloride 0.13 % Topical Solution
  • RxCUI: 2286262 - benzalkonium chloride 1.3 MG/ML / ethanol 0.7 ML/ML Topical Solution
  • RxCUI: 2286262 - benzalkonium chloride 0.13 % / ethanol 70 % Topical Solution

* Please review the disclaimer below.

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".