NDC 55455-007 Youjie Weishi Kitchen Cleaning 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:
55455-007
Proprietary Name:
Youjie Weishi Kitchen Cleaning Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hebei Youjie Weishi Technology Co., Ltd.
Labeler Code:
55455
Start Marketing Date: [9]
04-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Imprint(s):
YOUJIEWEISHI

Product Packages

NDC Code 55455-007-01

Package Description: 720 mL in 1 BOTTLE

Product Details

What is NDC 55455-007?

The NDC code 55455-007 is assigned by the FDA to the product Youjie Weishi Kitchen Cleaning 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 55455-007-01 720 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 Kitchen Cleaning Disinfectant?

Dilute the product in clean water at a dilution rate of 1:100 into a diluent for use, clean,immerse and/or wipe tableware/kitchen items with the diluent or spray the diluent onto tableware/kitchen items; let the diluent perform cleaning and disinfecting for 10 minutes, flush the tableware/kitchen items with running cleaning water or wipe them clean.

Which are Youjie Weishi Kitchen Cleaning Disinfectant UNII Codes?

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

Which are Youjie Weishi Kitchen Cleaning 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".