NDC 49967-123 - Kiehls Activated Sun Protector Sunscreen SPF 50 For Face and Body For All Skin Types

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

49967-123

Package NDCs from labels

49967-123-01, 49967-123-02

Manufacturer

L'Oreal USA Products Inc | Cosmetic Essence, LLC | Universal Packaging Systems, Inc.

Effective date

2026-01-07

Current FDA listing

Not matched in FDA.report NDC product tables