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  4. NDC Product Code: 82010-001 Deodorant Disinfectant Concentrate

NDC 82010-001 Deodorant Disinfectant Concentrate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82010-001?
  4. Deodorant Disinfectant Concentrate 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:
82010-001
Proprietary Name:
Deodorant Disinfectant Concentrate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yunbai (beijing) Technology Co.ltd
Labeler Code:
82010
Product Label ID:
c4654bfc-bc77-a972-e053-2a95a90a323d
Start Marketing Date: [9]
06-10-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82010-001-01

Package Description: 300 mL in 1 BOTTLE

Product Details

What is NDC 82010-001?

The NDC code 82010-001 is assigned by the FDA to the product Deodorant Disinfectant Concentrate which is product labeled by Yunbai (beijing) Technology Co.ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82010-001-01 300 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 Deodorant Disinfectant Concentrate?

Strong removal of odor in room and vehicleBacterial eliminating rate: 99.97% Kill rate of influenza A virus: Above 90% Strong mites removal, with mites removal rate: Above 81%Nontoxic according to oral test, no skin irritation

Which are Deodorant Disinfectant Concentrate UNII Codes?

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

Which are Deodorant Disinfectant Concentrate 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".