79208-001 NDC - ANTI-MICROBIAL ALCOHOL FREE HAND SANITIZER ()

Drug Information

Product NDC: 79208-001

Proprietary Name: Anti-microbial Alcohol Free Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Ultra Chem Labs
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/1/2020

Package Information

No. Package Code Package Description Billing Unit
179208-001-013785 mg in 1 BOTTLE (79208-001-01)
279208-001-32946 mg in 1 BOTTLE (79208-001-32)
379208-001-5050 mg in 1 BOTTLE (79208-001-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79208-001The 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 NAMEAnti-microbial Alcohol Free 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 DATE7/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUltra Chem LabsName 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