Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC.
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:32:16

Label at a glance#

ProductKiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution
Active ingredientDROMETRIZOLE TRISILOXANE, ECAMSULE, BEMOTRIZINOL, TITANIUM DIOXIDE, OCTINOXATE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE
Label structure4 sections

Dosage and administration

Apply in the morning at the end of your daily skincare routine. Avoid eye area. May be used alone or under a foundation. In case of contact with eyes, rinse immediately and thoroughly. When exposed to intense ot prolonged sun, use an adapted sunscreen.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Apply in the morning at the end of your daily skincare routine. Avoid eye area. May be used alone or under a foundation. In case of contact with eyes, rinse immediately and thoroughly. When exposed to intense ot prolonged sun, use an adapted sunscreen.

Ingredients

OTC - ACTIVE INGREDIENT SECTION

Drometrizole Trisiloxane, Terephthalylidene Dicamphor Sulfonic Acid, Bis-ethylhexyloxyphenol methoxyphenyl triazine, Titanium Dioxide, Ethylhexyl Methoxycinnamate, Diethylamino Hydroxybenzoyl Hexyl Benzoate

Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water, Butylene Glycol, Glycerin, Dimethicone, Isocetyl Stearate, Alcohol Denate., Propylene Glycol, Stearic Acid, Potassium Cetyl Phosphate, Tocopherol, Palmitic Acid, PEG-100 Stearate, Glyceryl Stearate, Phenoxyethanol, Cetyl alcohol, Cellulose, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Aluminum Hydroxide, Caprylyl Glycol, Sodium Cocoyl Sarcosinate, Carbomer, Scutellaria Baicalensis Extract/Scutellaria Baicalensis Root Extract, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Citric Acid, Isohexadecane, Xanthan Gum, Myristic Acid, Pelargonium Graveolens Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Disodium EDTA, Litchi Chinensis Pericarp Extract, Adenosine, Polysorbate 80, Ethylhexyl Hydroxystearate, Sorbitan Isostearate, Sorbitan Oleate, Polysorbate 60, BHT, Sodium Chloride. May Contain: CI77891/Titanium Dioxide, CI 77491, CI 77492, CI 77499/Iron Oxides, CI 77163/Bismuth Oxychloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image description
image description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-161-01Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution1 in 1 CARTONCREAM15
49967-161-01Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution30 mL in 1 TUBECREAM305
49967-161-02Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution5 mL in 1 TUBECREAM55
49967-161-03Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution3 mL in 1 PACKETCREAM35

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 43 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-16149967-161-01, 49967-161-02, 49967-161-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 41 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6495ce73-fcde-40e8-90b1-de1d368bd1a0fc89f98e-2b9f-4abd-84ce-2200e906db032026-01-07Exact identifier
spl id: 6495ce73-fcde-40e8-90b1-de1d368bd1a0
spl set id: fc89f98e-2b9f-4abd-84ce-2200e906db03

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.