OTC - ACTIVE INGREDIENT SECTION
OCTOCRYLENE 2%
OCTOCRYLENE 2%
SUNSCREEN
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right
away.
For external use only.
Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs.
When using this product keep out of eyes. Rinse with water to remove.
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
WATER, CYCLOPENTASILOXANE, METHKYPROPANEDIOL, CI 77891, SONONKY ISONONANOATE, LAURKY PEG-9 POLYDIMETHKYSILOXYETHKY DIMETHICONE, DIISOSTEARKY MALATE, CETKY PEG/PPG-10/1 DIMETHICONE, TRIMETHKYSILOXYSILICATE, SODIUM CHLORIDE, POLYETHKYENE, QUATERNIUM-18 BENTONITE, SODIUM HYDROXIDE, CI 77492, PHENOXYETHANOL, LAUROKY LYSINE, CI 77491, MICA, ALUMINA, DIPOTASSIUM GLYCYRRHIZATE, CI 77499, SODIUM HYALURONATE, FRAGRANCE, TRIETHOXYCAPRKYKYSILANE, GLYCYRRHIZA GLABRA EXTRACT, ETHKYHEXKY METHOXYCINNAMATE, ETHKYHEXKY SALICKYATE, PHENKYBENZIMIDAZOLE SULFONIC ACID, DIETHKYAMINO HYDROXYBENZOKY HEXKY BENZOATE.
Apply liberally 15 minutes before sun exposure • Reapply: • after 40 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months of age: ask a doctor
Helps prevent sunburn.If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
Universal Tinted Moisturizer
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 85530-368 | 85530-368-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CI 77491 | 1K09F3G675 | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| CI 77499 | XM0M87F357 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| MICA | V8A1AW0880 | IACT |
| ALUMINA | LMI26O6933 | IACT |
| CI 77492 | EX438O2MRT | IACT |
| SODIUM HYALURONATE | YSE9PPT4TH | IACT |
| QUATERNIUM-18 BENTONITE | 7F465U79Q1 | IACT |
| OCTOCRYLENE | 5A68WGF6WM | ACTIB |
| CYCLOPENTASILOXANE | 0THT5PCI0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| CI 77891 | 15FIX9V2JP | IACT |
| DIPOTASSIUM GLYCYRRHIZATE | CA2Y0FE3FX | IACT |
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 |
|---|---|---|---|---|---|---|
| 3fca98f4-424f-804f-e063-6394a90a389c | 32d4f4a7-a315-bcaa-e063-6394a90a560e | 2025-09-27 | Warnings | 32d4f4a7-a315-bcaa-e063-6394a90a560e |
Adverse event summaries are temporarily unavailable. Other product information remains available.