75738-004 NDC - BIOARMOUR HAND SANITIZER ()

Drug Information

Product NDC: 75738-004

Proprietary Name: BioArmour Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Ningbo Unice Houseware Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	4/28/2020

No.	Package Code	Package Description
1	75738-004-01	250 mL in 1 BOTTLE, PUMP (75738-004-01)
2	75738-004-02	500 mL in 1 BOTTLE, PUMP (75738-004-02)
3	75738-004-03	750 mL in 1 BOTTLE, PUMP (75738-004-03)
4	75738-004-04	1000 mL in 1 BOTTLE, PUMP (75738-004-04)
5	75738-004-05	1500 mL in 1 BOTTLE, PUMP (75738-004-05)
6	75738-004-06	2000 mL in 1 BOTTLE, PUMP (75738-004-06)
7	75738-004-07	2500 mL in 1 BOTTLE, PUMP (75738-004-07)
8	75738-004-08	3000 mL in 1 BOTTLE, PUMP (75738-004-08)
9	75738-004-09	3780 mL in 1 BOTTLE, PUMP (75738-004-09)
10	75738-004-10	4000 mL in 1 BOTTLE, PUMP (75738-004-10)
11	75738-004-11	5000 mL in 1 BOTTLE, PUMP (75738-004-11)

Field Name	Field Value	Definition
PRODUCT NDC	75738-004	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	BioArmour Hand Sanitizer	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	Squeeze hose	A 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 DATE	4/28/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Ningbo Unice Houseware Co., 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