NDC 21749-943 - GOJO Foaming Handsoap Crystal

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC

21749-943

Package NDCs from labels

21749-943-18, 21749-943-97, 21749-943-89

Manufacturer

GOJO Industries, Inc.

Effective date

2020-08-31

Current FDA listing

Not matched in FDA.report NDC product tables