NDC 50865-217 Health Guard Antibacterial Hand Cleanser F217f

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:
50865-217
Proprietary Name:
Health Guard Antibacterial Hand Cleanser F217f
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kutol Products Company
Labeler Code:
50865
Start Marketing Date: [9]
09-29-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50865-217-65

Package Description: 800 mL in 1 BAG

Product Details

What is NDC 50865-217?

The NDC code 50865-217 is assigned by the FDA to the product Health Guard Antibacterial Hand Cleanser F217f which is product labeled by Kutol Products Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50865-217-65 800 ml in 1 bag . 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 Health Guard Antibacterial Hand Cleanser F217f?

Uses For handwashing to decrease bacteria on the skin. Usos Para lavar las manos para disminuir las bacterias en la piel.

Which are Health Guard Antibacterial Hand Cleanser F217f UNII Codes?

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

Which are Health Guard Antibacterial Hand Cleanser F217f 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".