NDC 54749-001 Youke An

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:
54749-001
Proprietary Name:
Youke An
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hunan Zonwe Pharmaceutical Co., Ltd.
Labeler Code:
54749
Start Marketing Date: [9]
04-06-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - TRANSPARENT)

Product Packages

NDC Code 54749-001-01

Package Description: 60 mL in 1 BOTTLE

Product Details

What is NDC 54749-001?

The NDC code 54749-001 is assigned by the FDA to the product Youke An which is product labeled by Hunan Zonwe Pharmaceutical Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54749-001-01 60 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 Youke An?

It shall be directly sprayed onto skin, wounds, mucosa and infected parts. It can be applied several times a day to bring continuous antiseptic effects on skin surface for lasting protection.

Which are Youke An UNII Codes?

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

Which are Youke An 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".