NDC 74195-010 Clean And Hand

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:
Proprietary Name:
Clean And Hand
Product Type: [3]
Labeler Name: [5]
Opseve Korea Co.,ltd.
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 74195-010-01

Package Description: 25 mL in 1 POUCH

NDC Code 74195-010-02

Package Description: 100 mL in 1 BOTTLE

NDC Code 74195-010-03

Package Description: 500 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 74195-010?

The NDC code 74195-010 is assigned by the FDA to the product Clean And Hand which is product labeled by Opseve Korea Co.,ltd.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 74195-010-01 25 ml in 1 pouch , 74195-010-02 100 ml in 1 bottle , 74195-010-03 500 ml in 1 bottle, pump . 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 Clean And Hand?

Directions:Take an appropriate amount on your hands and rub thoroughly to dry.

Which are Clean And Hand UNII Codes?

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

Which are Clean And Hand 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 Clean And Hand?

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".