80849-001 NDC - HAPPY HANDS ()

Drug Information

Product NDC: 80849-001

Proprietary Name: HAPPY HANDS

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	American Ethanol Company, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	10/1/2020

No.	Package Code	Package Description
1	80849-001-01	118 mL in 1 BOTTLE, PLASTIC (80849-001-01)
2	80849-001-02	236 mL in 1 BOTTLE, PLASTIC (80849-001-02)
3	80849-001-03	473 mL in 1 BOTTLE, PLASTIC (80849-001-03)
4	80849-001-04	500 mL in 1 BOTTLE, PLASTIC (80849-001-04)
5	80849-001-05	946 mL in 1 BOTTLE, PLASTIC (80849-001-05)
6	80849-001-06	1000 mL in 1 BOTTLE, PLASTIC (80849-001-06)
7	80849-001-07	3000 mL in 1 BOTTLE, PLASTIC (80849-001-07)
8	80849-001-08	3785 mL in 1 BOTTLE, PLASTIC (80849-001-08)
9	80849-001-09	1040990 mL in 1 DRUM (80849-001-09)

Field Name	Field Value	Definition
PRODUCT NDC	80849-001	The 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 NAME	HAPPY HANDS	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	10/1/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	American Ethanol Company, LLC	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024