NDC 40796-003 Hands-free Surgical 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:
40796-003
Proprietary Name:
Hands-free Surgical Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
40796
Start Marketing Date: [9]
05-13-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Imprint(s):
ECONOMICAL

Code Structure Chart

Product Details

What is NDC 40796-003?

The NDC code 40796-003 is assigned by the FDA to the product Hands-free Surgical Gel which is product labeled by Jiangxi Baiyi Weishi Medical Technology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 40796-003-01 500 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 Hands-free Surgical Gel?

1. Disinfect external hands: Wash and dry your hands and forearms with soap solution, then take about 5min of thisproduct. Rub the hands and forearms evenly for 3 minutes according to the (disinfection technical specifications). Bacteria gloves. 2. Take 3ml of this product's original solution and rub it with your hands for 1 minute during inspection, treatment and nursing of patients. 3. Sanitize your hands after daily work: Take about 3ml of this product and rub your hands for 1 minute.

Which are Hands-free Surgical Gel UNII Codes?

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

Which are Hands-free Surgical 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".