NDC 54340-764 Berkley Jensen Hypoallergenic Antibacterial Hand Soap Soap Enriched With Vitamin E And Aloe Vera Moisturizers

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:
54340-764
Proprietary Name:
Berkley Jensen Hypoallergenic Antibacterial Hand Soap Soap Enriched With Vitamin E And Aloe Vera Moisturizers
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Dial Corporation
Labeler Code:
54340
Start Marketing Date: [9]
01-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54340-764-01

Package Description: 3780 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 54340-764?

The NDC code 54340-764 is assigned by the FDA to the product Berkley Jensen Hypoallergenic Antibacterial Hand Soap Soap Enriched With Vitamin E And Aloe Vera Moisturizers which is product labeled by The Dial Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54340-764-01 3780 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 Berkley Jensen Hypoallergenic Antibacterial Hand Soap Soap Enriched With Vitamin E And Aloe Vera Moisturizers?

This product is used as Uses - For handwashing to decrease bacteria on the skin

Which are Berkley Jensen Hypoallergenic Antibacterial Hand Soap Soap Enriched With Vitamin E And Aloe Vera Moisturizers UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Berkley Jensen Hypoallergenic Antibacterial Hand Soap Soap Enriched With Vitamin E And Aloe Vera Moisturizers?

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".