75569-200 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 75569-200

Proprietary Name: Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: The Hanson Group, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
175569-200-013785 mL in 1 JUG (75569-200-01)
275569-200-0218927 mL in 1 PAIL (75569-200-02)
375569-200-03196841 mL in 1 DRUM (75569-200-03)
475569-200-041010700 mL in 1 TANK (75569-200-04)
575569-200-051893 mL in 1 JUG (75569-200-05)
675569-200-0660 mL in 1 BOTTLE (75569-200-06)
775569-200-08120 mL in 1 BOTTLE (75569-200-08)
875569-200-09240 mL in 1 BOTTLE (75569-200-09)
975569-200-10480 mL in 1 BOTTLE (75569-200-10)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75569-200The 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 NAMEHand 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 NAMEThe Hanson Group, LLCName 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