78146-755 NDC - DR. ALPHA CLEAN HAND SANITIZER ()

Drug Information

Product NDC: 78146-755

Proprietary Name: Dr. Alpha Clean Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: EVESEL CO., LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
178146-755-103785 mL in 1 BOTTLE (78146-755-10)
278146-755-111000 mL in 1 BOTTLE (78146-755-11)
378146-755-12120 mL in 1 BOTTLE (78146-755-12)
478146-755-30300 mL in 1 BOTTLE (78146-755-30)
578146-755-50500 mL in 1 BOTTLE (78146-755-50)
678146-755-6060 mL in 1 BOTTLE (78146-755-60)

NDC Record

Field Name Field Value Definition
PRODUCT NDC78146-755The 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. Alpha Clean 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 DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEEVESEL 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