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  4. NDC Product Code: 52779-002 Compound Alcohol Hand Disinfection Gel

NDC 52779-002 Compound Alcohol Hand Disinfection Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52779-002?
  5. Compound Alcohol Hand Disinfection Gel 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:
52779-002
Proprietary Name:
Compound Alcohol Hand Disinfection Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Beijing Xidebao Disinfection Products Co. Ltd.
Labeler Code:
52779
Product Label ID:
a5ab96bf-bf7c-13fa-e053-2995a90a9f68
Start Marketing Date: [9]
05-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Imprint(s):
XIDEBAO

Code Structure Chart

Product Details

What is NDC 52779-002?

The NDC code 52779-002 is assigned by the FDA to the product Compound Alcohol Hand Disinfection Gel which is product labeled by Beijing Xidebao Disinfection Products Co. Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52779-002-01 500 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 Compound Alcohol Hand Disinfection Gel?

1. Surgical hand disinfection: for clean hands, put about 3 ml to 5 ml on palms, rub from hands to forearms, wait for 3 to 5 minutes. 2. Sanitary hand disinfection: put about 3 ml on palms,smear evenly over hands, wait for 1 minute.

Which are Compound Alcohol Hand Disinfection Gel UNII Codes?

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

Which are Compound Alcohol Hand Disinfection Gel 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".