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  4. NDC Product Code: 55455-005 Youjie Weishi Air Disinfectant

NDC 55455-005 Youjie Weishi Air Disinfectant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55455-005?
  5. Youjie Weishi Air Disinfectant 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:
55455-005
Proprietary Name:
Youjie Weishi Air Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hebei Youjie Weishi Technology Co., Ltd.
Labeler Code:
55455
Product Label ID:
a50a3c7c-49fb-706b-e053-2995a90a79db
Start Marketing Date: [9]
04-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Imprint(s):
YOUJIEWEISHI

Code Structure Chart

Product Details

What is NDC 55455-005?

The NDC code 55455-005 is assigned by the FDA to the product Youjie Weishi Air Disinfectant which is product labeled by Hebei Youjie Weishi Technology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55455-005-01 1000 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 Youjie Weishi Air Disinfectant?

Dilute this product in clean water at a dilution rate of 1:100 into a diluent for use as per a dosage of 10 mL per square meter (m); put the diluent into Youjie Weishi Air Disinfectant Atomizer; start the atomizer and keep it working for 45 minutes.

Which are Youjie Weishi Air Disinfectant UNII Codes?

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

Which are Youjie Weishi 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:

* Please review the disclaimer below.

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".