50865-213 NDC - FOAMING ADVANCED ANTIBACTERIAL HAND ()

Drug Information

Product NDC: 50865-213

Proprietary Name: Foaming Advanced Antibacterial Hand

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	50865-213-09	3875 mL in 1 BOTTLE (50865-213-09)
2	50865-213-10	1000 mL in 1 BAG (50865-213-10)
3	50865-213-13	3785 mL in 1 BOTTLE, PLASTIC (50865-213-13)
4	50865-213-14	950 mL in 1 BOTTLE (50865-213-14)
5	50865-213-17	50 mL in 1 BOTTLE, PLASTIC (50865-213-17)
6	50865-213-41	1000 mL in 1 BAG (50865-213-41)
7	50865-213-44	1000 mL in 1 BAG (50865-213-44)
8	50865-213-50	1200 mL in 1 BAG (50865-213-50)
9	50865-213-78	950 mL in 1 BOTTLE, PLASTIC (50865-213-78)

Field Name	Field Value	Definition
PRODUCT NDC	50865-213	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	Foaming Advanced Antibacterial Hand	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	10/1/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Kutol Products Company	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