79916-001 NDC - CLEAN SEPT ALCOHOL ANTISEPTIC 70% - TOPICAL HAND SANITIZER NON-STERILE GEL ()

Drug Information

Product NDC: 79916-001

Proprietary Name: Clean Sept Alcohol Antiseptic 70% - Topical Hand Sanitizer Non-Sterile Gel

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: BE FACTORY LABORATORIES INDUSTRIA COMERCIO IMPORTACAO E EXPORTACAO LTDA
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/6/2020

Package Information

No. Package Code Package Description Billing Unit
179916-001-01200 mL in 1 BOTTLE (79916-001-01)
279916-001-02500 mL in 1 BOTTLE (79916-001-02)
379916-001-031500 mL in 1 BOTTLE (79916-001-03)
479916-001-045000 mL in 1 JUG (79916-001-04)
579916-001-053 mL in 1 POUCH (79916-001-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79916-001The 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 NAMEClean Sept Alcohol Antiseptic 70% - Topical Hand Sanitizer Non-Sterile GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/6/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBE FACTORY LABORATORIES INDUSTRIA COMERCIO IMPORTACAO E EXPORTACAO LTDAName 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