42719-346 NDC - BYOTROL ANTIBACTERIAL FOAMING HAND SANITIZER ()

Drug Information

Product NDC: 42719-346

Proprietary Name: Byotrol Antibacterial Foaming Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	42719-346-06	1250 mL in 1 CARTRIDGE (42719-346-06)
2	42719-346-50	500 mL in 1 BOTTLE (42719-346-50)
3	42719-346-51	210 mL in 1 BOTTLE (42719-346-51)
4	42719-346-99	50 mL in 1 BOTTLE (42719-346-99)

Field Name	Field Value	Definition
PRODUCT NDC	42719-346	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Byotrol Antibacterial Foaming Hand Sanitizer	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	3/8/2013	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Byotrol, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023