OTC Medication Information: KIEHLS DERMATOLOGIST SOLUTIONS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN SPF 50 HIGH PROTECTION ANTI-POLLUTION LIGHTWEIGHT FORMULA FOR ALL SKIN TYPES

KIEHLS DERMATOLOGIST SOLUTIONS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN SPF 50 HIGH PROTECTION ANTI-POLLUTION LIGHTWEIGHT FORMULA FOR ALL SKIN TYPES- drometrizole trisiloxane, titanium dioxide, ecamsule, bemotrizinol, diethylamino hydroxybenzoyl hexyl benzoate and octinoxate lotion
L’Oreal USA Products, Inc.

Ingredients

Drometrizole Trisiloxane

Titanium Dioxide

Terephthalylidene Dicamphor Sulfonic Acid

Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine

Diethylamino Hydroxybenzoyl Hexyl Benzoate

Ethylhexyl Methoxycinnamate

Inactive ingredients

-Aqua/Water, Glycerin, Propylene Glycol, Alcohol Denat., Triethanolamine, Stearic Acid, Potassium Cetyl Phosphate, Nylon-12, Palmitic Acid, PEG-100 Stearate, Glyceryl Stearate, Phenoxyethanol, Cetyl Alcohol, Cellulose, Citric Acid, Aluminum Hydroxide, Caprylyl Glycol, Sodium Cocoyl Sarcosinate, Carbomer, Tocopherol, Tromethanime, Scutellaria Baicalensis Extract/Scutellaria Baicalensis Root Extract, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Isohexadecane, Xanthan Gum, Myristic Acid, Disodium EDTA, Adenosine, Polysorbate 80, Arginine, Mannitol, Disodium Adenosine Triphosphate, RNA, Pyridoxane HCL, Sorbitan Oleate, Sorbitol, Pentylene Glycol, BHT, Histidine HCL, Zea Mays Kernel Extract/Corn Kernel Extract, Sodium Chloride, Faex Extract/Yeast Extract, Phenylalanine, Mentha Piperita Extract/Perppermint Extract, Rosa Gallica Flower Extract, Tyrosine, Sorbic Acid

Directions

Apply in the morning at the end of your daily skincare routine. Avoid eye area. In case of contact with eyes, rinse immediately and thoroughly.

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KIEHLS DERMATOLOGIST SOLUTIONS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN SPF 50 HIGH PROTECTION ANTI-POLLUTION LIGHTWEIGHT FORMULA FOR ALL SKIN TYPES
drometrizole trisiloxane, titanium dioxide, ecamsule, bemotrizinol, diethylamino hydroxybenzoyl hexyl benzoate and octinoxate lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NHRIC:49967-449
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DROMETRIZOLE TRISILOXANE (DROMETRIZOLE TRISILOXANE) DROMETRIZOLE TRISILOXANE 40 mg in 1 mL
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE 40 mg in 1 mL
ECAMSULE (ECAMSULE) ECAMSULE 120 mg in 1 mL
BEMOTRIZINOL (BEMOTRIZINOL) BEMOTRIZINOL 5 mg in 1 mL
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 5 mg in 1 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE 67.5 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
DIMETHICONE
GLYCERIN
PROPYLENE GLYCOL
ALCOHOL
TROLAMINE
STEARIC ACID
POTASSIUM CETYL PHOSPHATE
NYLON-12
PALMITIC ACID
PEG-100 STEARATE
GLYCERYL MONOSTEARATE
PHENOXYETHANOL
CETYL ALCOHOL
POWDERED CELLULOSE
CITRIC ACID MONOHYDRATE
ALUMINUM HYDROXIDE
CAPRYLYL GLYCOL
SODIUM COCOYL SARCOSINATE
CARBOXYPOLYMETHYLENE
TOCOPHEROL
TROMETHAMINE
SCUTELLARIA BAICALENSIS ROOT
ISOHEXADECANE
XANTHAN GUM
MYRISTIC ACID
EDETATE DISODIUM
ADENOSINE
POLYSORBATE 80
ARGININE
MANNITOL
ADENOSINE TRIPHOSPHATE DISODIUM
PYRIDOXINE HYDROCHLORIDE
SORBITAN MONOOLEATE
SORBITOL
PENTYLENE GLYCOL
BUTYLATED HYDROXYTOLUENE
HISTIDINE MONOHYDROCHLORIDE
CORN
SODIUM CHLORIDE
YEAST, UNSPECIFIED
PHENYLALANINE
MENTHA PIPERITA
ROSA GALLICA FLOWER
TYROSINE
SORBIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NHRIC:49967-449-01 1 TUBE in 1 CARTON contains a TUBE
1 60 mL in 1 TUBE This package is contained within the CARTON (49967-449-01)
2 NHRIC:49967-449-02 1 TUBE in 1 CARTON contains a TUBE
2 30 mL in 1 TUBE This package is contained within the CARTON (49967-449-02)
3 NHRIC:49967-449-03 5 mL in 1 TUBE None
4 NHRIC:49967-449-04 3 mL in 1 PACKET None
5 NHRIC:49967-449-05 1.5 mL in 1 PACKET None
6 NHRIC:49967-449-06 10 mL in 1 TUBE None
7 NHRIC:49967-449-07 100 mL in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
export only 12/01/2017
Labeler — L’Oreal USA Products, Inc. (002136794)
Establishment
Name Address ID/FEI Operations
L’OREAL USA, INC. 185931458 manufacture (49967-449), pack (49967-449)

Revised: 12/2023 L’Oreal USA Products, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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