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  4. NDC Product Code: 79158-003 Hba Anti Bacterial Liquid

NDC 79158-003 Hba Anti Bacterial Liquid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79158-003?
  4. Hba Anti Bacterial Liquid Uses
  5. Active Ingredients UNII Codes
  6. 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:
79158-003
Proprietary Name:
Hba Anti Bacterial Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Henan Huibo Medical Co., Ltd.
Labeler Code:
79158
Product Label ID:
6cc9a531-4e8e-453c-80c8-c71b1bc8dff6
Start Marketing Date: [9]
07-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 79158-003?

The NDC code 79158-003 is assigned by the FDA to the product Hba Anti Bacterial Liquid which is product labeled by Henan Huibo Medical Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79158-003-01 100 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 Hba Anti Bacterial Liquid?

Spray the product directly on the skin, no need to washImmerse a piece of gauze in the disinfectant, then wipe the site of action repeatedly or do wet compressWhen disinfect the objects which have direct contact with skin, just spray the product directly

Which are Hba Anti Bacterial Liquid UNII Codes?

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

Which are Hba Anti Bacterial Liquid 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".