75615-0020 NDC - DR.BETTER HOMES HAND SANITIZER ()

Drug Information

Product NDC: 75615-0020

Proprietary Name: Dr.Better Homes HAND SANITIZER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: UI COSMETICS CO., LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/8/2020

Package Information

No. Package Code Package Description Billing Unit
175615-0020-010000 mL in 1 BOTTLE, PUMP (75615-0020-0)
275615-0020-1500 mL in 1 BOTTLE, PUMP (75615-0020-1)
375615-0020-250 mL in 1 BOTTLE (75615-0020-2)
475615-0020-360 mL in 1 BOTTLE (75615-0020-3)
575615-0020-4100 mL in 1 BOTTLE (75615-0020-4)
675615-0020-5200 mL in 1 BOTTLE, PUMP (75615-0020-5)
775615-0020-6250 mL in 1 BOTTLE, PUMP (75615-0020-6)
875615-0020-7300 mL in 1 BOTTLE, PUMP (75615-0020-7)
975615-0020-85000 mL in 1 BOTTLE, PUMP (75615-0020-8)
1075615-0020-93785 mL in 1 BOTTLE (75615-0020-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75615-0020The 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 NAMEDr.Better Homes 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 DATE5/8/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUI COSMETICS CO., LTDName 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