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Drug Information

Product NDC: 20276-163

Proprietary Name: Lucky Antibacterial Hand Soap

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Delta Brands Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/1/2010

Package Information

No. Package Code Package Description Billing Unit
120276-163-08237 mL in 1 BOTTLE, PUMP (20276-163-08)
220276-163-09266 mL in 1 BOTTLE, PUMP (20276-163-09)
320276-163-10296 mL in 1 BOTTLE, PUMP (20276-163-10)
420276-163-11333 mL in 1 BOTTLE, PUMP (20276-163-11)
520276-163-12355 mL in 1 BOTTLE, PUMP (20276-163-12)
620276-163-13400 mL in 1 BOTTLE, PUMP (20276-163-13)
720276-163-14414 mL in 1 BOTTLE, PUMP (20276-163-14)
820276-163-15444 mL in 1 BOTTLE, PUMP (20276-163-15)
920276-163-16500 mL in 1 BOTTLE, PUMP (20276-163-16)
1020276-163-32946 mL in 1 BOTTLE, PLASTIC (20276-163-32)
1120276-163-401183 mL in 1 BOTTLE, PLASTIC (20276-163-40)
1220276-163-75222 mL in 1 BOTTLE, SPRAY (20276-163-75)

NDC Record

Field Name Field Value Definition
PRODUCT NDC20276-163The 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 NAMELucky Antibacterial Hand SoapThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXSupersoftA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE9/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDelta Brands IncName 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