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  4. NDC Product Code: 53042-002 Luobenqing Surgical Hand Sanitizer

NDC 53042-002 Luobenqing Surgical Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 53042-002?
  5. Luobenqing Surgical Hand Sanitizer Uses
  6. Active Ingredients UNII Codes
  7. 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:
53042-002
Proprietary Name:
Luobenqing Surgical Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lustre Pharmaceutical Lab.co.,ltd.
Labeler Code:
53042
Product Label ID:
a21314e9-5445-f410-e053-2995a90a6736
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 53042-002-01

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 53042-002?

The NDC code 53042-002 is assigned by the FDA to the product Luobenqing Surgical 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 53042-002-01 500 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 Luobenqing Surgical Hand Sanitizer?

Please washandbrushyour hands as usual, and dry with a sterile towel (soapresidual prohibited).Then take 5ml or more of this product and knead for 5 minutes.

Which are Luobenqing Surgical Hand Sanitizer UNII Codes?

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

Which are Luobenqing Surgical 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".