Drug Facts

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:08

Label at a glance#

ProductKIEHLS ACTIVATED SUN PROTECTOR ULTRA LIGHT SUNSCREEN SPF 50 FOR BODY SWEAT AND WATER RESISTANT
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTISALATE, TITANIUM DIOXIDE, ECAMSULE
Label structure1 sections

Label contents#

Full prescribing information#

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 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-98649967-986-01

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
ee431cdf-5e50-47d6-91f6-47f4fae2629b6f288e79-1e06-41d9-a4da-263a7cc107412023-01-27Exact identifier
spl set id: 6f288e79-1e06-41d9-a4da-263a7cc10741

Reported adverse events (FAERS/openFDA)#

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