Home NDC 49967-309 NDC 49967-309 - Kiehls Activated Sun Protector Sunscreen SPF 30 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 49967-309
Package NDCs from labels 49967-309-01, 49967-309-02
Manufacturer L'Oreal USA Products Inc | Cosmetic Essence, LLC
Effective date 2026-01-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-309-01 Kiehls Activated Sun Protector Sunscreen SPF 30 For Face and Body For All Skin Types 150 mL in 1 TUBE LOTION 150 7 49967-309-02 Kiehls Activated Sun Protector Sunscreen SPF 30 For Face and Body For All Skin Types 5 mL in 1 PACKET LOTION 5 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-309 KIEHLS ACTIVATED SUN PROTECTOR SUNSCREEN SPF 30 FOR FACE AND BODY FOR ALL SKIN TYPES (ETHYLHEXYL TRIAZONE, DROMETRIZOLE TRISILOXANE, HOMOSALATE, TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID, ETHYLHEXYL SALICYLATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE AND DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE) LOTION [L'OREAL USA PRODUCTS INC] 6 2 package rows 20241228_38ea04f6-ebb7-46b3-a157-7ce1271deb1f.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 218 of 326 · 6,520 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.