Drug Facts

Manufacturer
L'Oreal USA Products Inc | Cosmetic Essence, LLC
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:31:59

Label at a glance#

ProductKiehls Activated Sun Protector Sunscreen SPF 30 For Face and Body For All Skin Types
Active ingredientETHYLHEXYL TRIAZONE, DROMETRIZOLE TRISILOXANE, HOMOSALATE, ECAMSULE, OCTISALATE, BEMOTRIZINOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE
Label structure4 sections

Dosage and administration

Apply liberally and evenly onto face and/or body prior to sun exposure and massage into skin for complete coverage. Avoid the eye area. Leave ot dry and apply a second time to ensure a generous application. An insufficient amount of product reduces the level of protection. Re-apply frequently to maintain protection, especially after swimming, perspiring, or using a towel. Over-exposure to tht sun is dangerous. Kee...

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally and evenly onto face and/or body prior to sun exposure and massage into skin for complete coverage. Avoid the eye area. Leave ot dry and apply a second time to ensure a generous application. An insufficient amount of product reduces the level of protection. Re-apply frequently to maintain protection, especially after swimming, perspiring, or using a towel. Over-exposure to tht sun is dangerous. Keep babies and young children out of direct sunlight, and well covered. Do not stay too long in the sun, even while using a sunscreen product, because it does not provide you 100% protection. In case of contact with eyes, rinse them immediately and thoroughly.

Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Triazone, Drometrizole Trisiloxane, Homosalate, Terephthalylidene Dicamphor Sulfonic Acid, Ethyhexyl Salicylate, Bis-Ethylhexyloxyphenol methoxyphenyl triazine, Diethylamino hydroxybenzoyl hexyl benzoate

Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water, Glycerin, C12-15 Alkyl Benzoate, Alcohol Denat., Zea Mays Starch/Corn Starch, Propylene Glycol, Synthetic Wax, Sulfonic Acid, Stearic Acid, Palmitic Acid, PEG-100 Stearate, Glyceryl Stearate, Parfum/Fragrance, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Stearoyl Glutamate, Glycine Soja Oil/Soybean Oil, Tocopherol, Xanthan Gum, Benzyl Salicylate, Benzyl Alcohol, Myristic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-309-01Kiehls Activated Sun Protector Sunscreen SPF 30 For Face and Body For All Skin Types150 mL in 1 TUBELOTION1507
49967-309-02Kiehls Activated Sun Protector Sunscreen SPF 30 For Face and Body For All Skin Types5 mL in 1 PACKETLOTION57

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-30949967-309-01, 49967-309-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 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
8f0f139a-c83d-4a45-ba44-bea92d45c0bf38ea04f6-ebb7-46b3-a157-7ce1271deb1f2026-01-07Exact identifier
spl id: 8f0f139a-c83d-4a45-ba44-bea92d45c0bf
spl set id: 38ea04f6-ebb7-46b3-a157-7ce1271deb1f

Reported adverse events (FAERS/openFDA)#

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