NDC 42091-002 Dr. Zheng S Acteriostatic Gel

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:
42091-002
Proprietary Name:
Dr. Zheng S Acteriostatic Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
42091
Start Marketing Date: [9]
04-11-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 42091-002?

The NDC code 42091-002 is assigned by the FDA to the product Dr. Zheng S Acteriostatic Gel which is product labeled by Guangzhou Yuxiao Biological Products Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42091-002-01 500 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 Dr. Zheng S Acteriostatic Gel?

Hand sanitization:take this product in the palm of your hand,and coat each part evenly with your hands for 1 minute.Disinfection of operation hand: clean and dry the hands,forearms and 1/ 3 of the lower part of the upper arm according to the specification, take 5-10g of this product and evenly spreadit on the hands, forearms and the lower part of the upper arm,rub it until it is dry, function for 3 minutes, and then wear sterilegloves. Hand disinfection in daily work: take 3G of this product andknead it for 1 minute.

Which are Dr. Zheng S Acteriostatic Gel UNII Codes?

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

Which are Dr. Zheng S Acteriostatic Gel 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".