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Drug Facts

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC.
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:32:11

Label at a glance#

ProductKIEHLS ULTRA LIGHT DAILY UV DEFENSE TONE UP SPF 50 ANTI POLLUTION INSTANTLY BRIGHTENS AND HYDRATES
Active ingredientECAMSULE, OCTINOXATE, TITANIUM DIOXIDE
Label structure2 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#

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

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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
49967-762-01KIEHLS ULTRA LIGHT DAILY UV DEFENSE TONE UP SPF 50 ANTI POLLUTION INSTANTLY BRIGHTENS AND HYDRATES30 mL in 1 TUBECREAM306
49967-762-02KIEHLS ULTRA LIGHT DAILY UV DEFENSE TONE UP SPF 50 ANTI POLLUTION INSTANTLY BRIGHTENS AND HYDRATES5 mL in 1 TUBECREAM56
49967-762-03KIEHLS ULTRA LIGHT DAILY UV DEFENSE TONE UP SPF 50 ANTI POLLUTION INSTANTLY BRIGHTENS AND HYDRATES3 mL in 1 PACKETCREAM36

Products#

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

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-76249967-762-01, 49967-762-02, 49967-762-03

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 44 matching rows.

Name, UNII, Kind table
NameUNIIKind
ECAMSULEM94R1PM439ACTIB
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
TROLAMINE9O3K93S3TKIACT
ADENOSINEK72T3FS567IACT
SORBITAN MONOOLEATE06XEA2VD56IACT
ISOHEXADECANE918X1OUF1EIACT
WATER059QF0KO0RIACT
POLYSORBATE 806OZP39ZG8HIACT
DIMETHICONE92RU3N3Y1OIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
POLYSORBATE 60CAL22UVI4MIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DISODIUM STEAROYL GLUTAMATE45ASM2L11MIACT
ALCOHOL3K9958V90MIACT
SODIUM COCOYL SARCOSINATE1R9DUY89CZIACT
SODIUM CHLORIDE451W47IQ8XIACT
ISOCETYL STEARATE3RJ7186O9WIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
EDETATE DISODIUM7FLD91C86KIACT
TOCOPHEROLR0ZB2556P8IACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
XANTHAN GUMTTV12P4NEEIACT
ETHYLHEXYL HYDROXYSTEARATEB7I80BVV5EIACT
BISMUTH OXYCHLORIDE4ZR792I587IACT
PELARGONIUM GRAVEOLENS FLOWER OIL3K0J1S7QGCIACT
ORANGE OILAKN3KSD11BIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
CETYL ALCOHOL936JST6JCNIACT
LITCHI FRUITY5P61KP51EIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
POWDERED CELLULOSESMD1X3XO9MIACT
MYRISTIC ACID0I3V7S25AWIACT

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
693f18d8-068e-4f43-8881-f87c531e5241dd38fcaa-007e-4f0d-a9c5-a3f06aee09722026-01-07Exact identifier
spl id: 693f18d8-068e-4f43-8881-f87c531e5241
spl set id: dd38fcaa-007e-4f0d-a9c5-a3f06aee0972

Reported adverse events (FAERS/openFDA)#

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