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Drug Facts

Manufacturer
L'Oreal USA Products, Inc. | L'OREAL USA, INC.
Effective date
2023-01-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:38:51

Label at a glance#

ProductKiehls Since 1851 Dermatologist Solutions Ultra Light Daily UV Defense Tone Up SPF 50 PA Plus Plus Plus Plus Antipoll...
Active ingredientDROMETRIZOLE TRISILOXANE, TITANIUM DIOXIDE, ECAMSULE, BEMOTRIZINOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, OCTINOXATE
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 or prolonged sun, use an adapted sunscreen.

Label contents#

Full prescribing information#

Ingredients

OTC - ACTIVE INGREDIENT SECTION

Drometrizole Trisiloxane

Titanium Dioxide

Terephthalylidene Dicamphor Sulfonic Acid

Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine

Diethylamino Hydroxybenzoyl Hexyl Benzoate

Ethylhexyl Methoxycinnamate

Ingredients

INACTIVE INGREDIENT SECTION

aqua/water, dimethicone, butylene glycol, glycerin, isocetyl stearate, alcohol denat., propylene glycol, triethanolamine, 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, disodium stearoyl glutamate, xanthan gum, ci 77163/bismuth oxychloride, myristic acid, pelargonium graveolens flower oil, citral

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 or prolonged sun, use an adapted sunscreen.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

Products#

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

DailyMed product names page 1 of 2 · 53 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-99149967-991-01, 49967-991-02, 49967-991-03

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 51 matching rows.

Name, UNII, Kind table
NameUNIIKind
DROMETRIZOLE TRISILOXANEHC22845I1XACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
ECAMSULEM94R1PM439ACTIB
BEMOTRIZINOLPWZ1720CBHACTIB
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20ACTIB
OCTINOXATE4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXIACT
ISOCETYL STEARATE3RJ7186O9WIACT
ALCOHOL3K9958V90MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
STEARIC ACID4ELV7Z65APIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
TOCOPHEROLR0ZB2556P8IACT
PALMITIC ACID2V16EO95H1IACT
PEG-100 STEARATEYD01N1999RIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
CETYL ALCOHOL936JST6JCNIACT
POWDERED CELLULOSESMD1X3XO9MIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
CAPRYLYL GLYCOL00YIU5438UIACT
SODIUM COCOYL SARCOSINATE1R9DUY89CZIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
ISOHEXADECANE918X1OUF1EIACT
DISODIUM STEAROYL GLUTAMATE45ASM2L11MIACT
XANTHAN GUMTTV12P4NEEIACT
BISMUTH OXYCHLORIDE4ZR792I587IACT
MYRISTIC ACID0I3V7S25AWIACT
PELARGONIUM GRAVEOLENS FLOWER OIL3K0J1S7QGCIACT
ORANGE OIL, COLD PRESSEDAKN3KSD11BIACT
EDETATE DISODIUM7FLD91C86KIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LITCHI FRUITY5P61KP51EIACT
ADENOSINEK72T3FS567IACT

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
c9ce31a4-6d32-4fe2-afb5-8a741a579a4a1b39070e-10e5-4ace-b9b6-7ecd76cd9a932023-01-27Exact identifier
spl id: c9ce31a4-6d32-4fe2-afb5-8a741a579a4a
spl set id: 1b39070e-10e5-4ace-b9b6-7ecd76cd9a93

Reported adverse events (FAERS/openFDA)#

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