50865-688 NDC - EZFOAM FOAMING ALCOHOL HAND SANITIZER ()

Drug Information

Product NDC: 50865-688

Proprietary Name: eZFoam Foaming Alcohol Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Kutol Products Company, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/27/2013

Package Information

No. Package Code Package Description Billing Unit
150865-688-093785 mL in 1 JUG (50865-688-09)
250865-688-1750 mL in 1 BOTTLE, PLASTIC (50865-688-17)
350865-688-241000 mL in 1 BAG (50865-688-24)
450865-688-411000 mL in 1 BAG (50865-688-41)
550865-688-501200 mL in 1 BAG (50865-688-50)
650865-688-78950 mL in 1 BOTTLE, PLASTIC (50865-688-78)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50865-688The 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 NAMEeZFoam Foaming Alcohol Hand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/27/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKutol Products Company, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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