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#
Products#
Every source-derived product name is available through these pages.
- KIEHLS ACTIVATED SUN PROTECTOR ULTRA LIGHT SUNSCREEN SPF 50 FOR BODY SWEAT AND WATER RESISTANT
- Octocrylene, octisalate, avobenzone, ecamsule and titanium dioxide
- OCTOCRYLENE
- AVOBENZONE
- OCTISALATE
- TITANIUM DIOXIDE
- ECAMSULE
- STEARIC ACID
- GLYCERYL MONOSTEARATE
- PEG-100 STEARATE
- DIMETHICONE
- ALKYL (C12-15) BENZOATE
- POTASSIUM CETYL PHOSPHATE
- BEMOTRIZINOL
- CAPRYLYL GLYCOL
- GLYCERIN
- PROPYLENE GLYCOL
- TOCOPHEROL
- PHENOXYETHANOL
- TROLAMINE
- STARCH, CORN
- WATER
- EDETATE DISODIUM
- ISOHEXADECANE
- XANTHAN GUM
- LYCIUM BARBARUM FRUIT
- NYLON-12
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49967-986 | 49967-986-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ee431cdf-5e50-47d6-91f6-47f4fae2629b | 6f288e79-1e06-41d9-a4da-263a7cc10741 | 2023-01-27 | 6f288e79-1e06-41d9-a4da-263a7cc10741 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
