Home NDC 49967-161 NDC 49967-161 - Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution 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 49967-161
Package NDCs from labels 49967-161-01, 49967-161-02, 49967-161-03
Manufacturer L'Oreal USA Products Inc | L'OREAL USA, INC.
Effective date 2026-01-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Drug Facts L'Oreal USA Products Inc | L'OREAL USA, INC. 2026-01-07 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-161-01 Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution 1 in 1 CARTON CREAM 1 5 49967-161-01 Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution 30 mL in 1 TUBE CREAM 30 5 49967-161-02 Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution 5 mL in 1 TUBE CREAM 5 5 49967-161-03 Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution 3 mL in 1 PACKET CREAM 3 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-161 KIEHLS ULTRA LIGHT DAILY UV DEFENSE CC SPF 50 ANTI POLLUTION (DROMETRIZOLE TRISILOXANE, TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE AND DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE) CREAM [L'OREAL USA PRODUCTS INC] 4 4 package rows 20231231_fc89f98e-2b9f-4abd-84ce-2200e906db03.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 4 of 391 · 7,812 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.