65601-800 NDC - ADVANCED ALCOHOL FOAMING HAND SANITIZER ()

Drug Information

Product NDC: 65601-800

Proprietary Name: Advanced Alcohol Foaming Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Betco Corporation, Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
165601-800-03750 mL in 1 BOTTLE (65601-800-03)
265601-800-043780 mL in 1 BOTTLE (65601-800-04)
365601-800-291000 mL in 1 BAG (65601-800-29)
465601-800-5350 mL in 1 BOTTLE, PUMP (65601-800-53)
565601-800-55208198 mL in 1 DRUM (65601-800-55)
665601-800-57550 mL in 1 BOTTLE, PUMP (65601-800-57)
765601-800-88500 mL in 1 BOTTLE, PUMP (65601-800-88)

NDC Record

Field Name Field Value Definition
PRODUCT NDC65601-800The 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 NAMEAdvanced Alcohol Foaming 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 DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBetco Corporation, Ltd.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