NDC 49351-202 Tork Foam Antibacterial

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:
49351-202
Proprietary Name:
Tork Foam Antibacterial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Essity North America Inc.
Labeler Code:
49351
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49351-202-01

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 49351-202?

The NDC code 49351-202 is assigned by the FDA to the product Tork Foam Antibacterial which is product labeled by Essity North America Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49351-202-01 1000 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 Tork Foam Antibacterial?

Wet hands, dispense enough to cover both hands, rub for 30 seconds then rinse with water for 30 seconds.

Which are Tork Foam Antibacterial UNII Codes?

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

Which are Tork Foam Antibacterial 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 Tork Foam Antibacterial?

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".