61139-513 NDC - HIGHMARK PROFESSIONAL PREMIUM FOAM ANTIBACTERIAL HANDWASH ()

Drug Information

Product NDC: 61139-513

Proprietary Name: Highmark Professional Premium Foam Antibacterial Handwash

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Office Max, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/22/2013

Package Information

No. Package Code Package Description Billing Unit
161139-513-101000 mL in 1 BOTTLE (61139-513-10)
261139-513-202000 mL in 1 BOTTLE (61139-513-20)
361139-513-80800 mL in 1 BAG (61139-513-80)
461139-513-891200 mL in 1 BOTTLE (61139-513-89)
561139-513-901250 mL in 1 BOTTLE (61139-513-90)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61139-513The 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 NAMEHighmark Professional Premium Foam Antibacterial HandwashThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/22/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOffice Max, 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