77871-002 NDC - 1SOURCE ADVANCED HAND SANITIZER LIQUID FOAM ()

Drug Information

Product NDC: 77871-002

Proprietary Name: 1SOURCE Advanced Hand Sanitizer Liquid Foam

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: AVS Energy Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/15/2020

Package Information

No. Package Code Package Description Billing Unit
177871-002-0160 mL in 1 BOTTLE (77871-002-01)
277871-002-02100 mL in 1 BOTTLE (77871-002-02)
377871-002-03237 mL in 1 BOTTLE (77871-002-03)
477871-002-04500 mL in 1 BOTTLE (77871-002-04)
577871-002-051000 mL in 1 BOTTLE (77871-002-05)
677871-002-062000 mL in 1 BOTTLE (77871-002-06)
777871-002-073785 mL in 1 BOTTLE (77871-002-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC77871-002The 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 NAME1SOURCE Advanced Hand Sanitizer Liquid FoamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/15/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAVS Energy IncName 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