NDC 73140-0004 Patchfetch Clean-k Medi Cure Sanitizer

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:
73140-0004
Proprietary Name:
Patchfetch Clean-k Medi Cure Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Times Co., Ltd.
Labeler Code:
73140
Start Marketing Date: [9]
03-04-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73140-0004-1

Package Description: 100 mL in 1 BOTTLE

Product Details

What is NDC 73140-0004?

The NDC code 73140-0004 is assigned by the FDA to the product Patchfetch Clean-k Medi Cure Sanitizer which is product labeled by The Times Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73140-0004-1 100 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 Patchfetch Clean-k Medi Cure Sanitizer?

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.Supervise children in the use of this product.

Which are Patchfetch Clean-k Medi Cure Sanitizer UNII Codes?

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

Which are Patchfetch Clean-k Medi Cure Sanitizer 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:

What is the NDC to RxNorm Crosswalk for Patchfetch Clean-k Medi Cure Sanitizer?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".