NDC 75348-004 Virapro Kids Hand Cleanser

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:
75348-004
Proprietary Name:
Virapro Kids Hand Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
All One Kozmetik Sanayi Dis Ticaret Anonim Sirketi
Labeler Code:
75348
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 75348-004-01

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 75348-004-02

Package Description: 100 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 75348-004?

The NDC code 75348-004 is assigned by the FDA to the product Virapro Kids Hand Cleanser which is product labeled by All One Kozmetik Sanayi Dis Ticaret Anonim Sirketi. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 75348-004-01 50 ml in 1 bottle, plastic , 75348-004-02 100 ml in 1 bottle, plastic . 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 Virapro Kids Hand Cleanser?

Squeeze a drop onto the palm of your hands. Rub your hands well and let them dry.

Which are Virapro Kids Hand Cleanser UNII Codes?

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

Which are Virapro Kids Hand Cleanser 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:

* Please review the disclaimer below.

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".