NDC 55455-004 Youjie Weishi 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:
55455-004
Proprietary Name:
Youjie Weishi Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
55455
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 55455-004?

The NDC code 55455-004 is assigned by the FDA to the product Youjie Weishi 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 55455-004-01 420 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 Disinfectant?

This product is applicable for: disinfection of hands and skin of medical staff in various hospital/healthcare departments such as medical surgery, obstetrics and gynecology detection, ICU, CCU, etc., disinfection of hands before and after work for workers in industries requiring clean production such as industries of pharmaceuticals, food, cosmetics, etc.; and disinfection oral mucosa, vaginal mucosa and skin mucosa.

Which are Youjie Weishi Disinfectant UNII Codes?

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

Which are Youjie Weishi 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".