NDC 55090-001 Chlorine Dioxide Air Disinfectant

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:
55090-001
Proprietary Name:
Chlorine Dioxide Air Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.
Labeler Code:
55090
Start Marketing Date: [9]
05-06-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 55090-001-01

Package Description: 6.5 g in 1 BOTTLE

Product Details

What is NDC 55090-001?

The NDC code 55090-001 is assigned by the FDA to the product Chlorine Dioxide Air Disinfectant which is product labeled by Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55090-001-01 6.5 g 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 Chlorine Dioxide Air Disinfectant?

Open the box and aluminum foil bag,according to the configuration of 1m/unit enclosed space, the operation time is 1h

Which are Chlorine Dioxide Air Disinfectant UNII Codes?

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

Which are Chlorine Dioxide Air Disinfectant 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".