Indications and uses
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
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
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 of 15 or higher and other sun protection measures including: limit time in the sun, ...
Avobenzone 1.9%, Octisalate 4.0%, Octocrylene 7.6%
Sunscreen
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
For external use only
Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask doctor if skin rash occurs
Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away.
apply liberally 15 minutes before sun exposure
reapply:
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 of 15 or higher and other sun protection measures including:
children under 6 months: Ask a doctor
Butyloctyl Salicylate, Dimethicone Crosspolymer, Flavor, Glycyrrhiza Glabra (Licorice) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, Iris Pallida Leaf Cell Extract, Isododecane, Lonicera Japonica Callus Extract, Nymphaea Alba Leaf Cell Extract, Withania Somnifera Root Extract
Protect this product from excessive heat and direct sun
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 76150-207 | 76150-207-33 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| AVOBENZONE | G63QQF2NOX | ACTIB |
| OCTOCRYLENE | 5A68WGF6WM | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| ISODODECANE | A8289P68Y2 | IACT |
| BUTYLOCTYL SALICYLATE | 2EH13UN8D3 | IACT |
| SUNFLOWER OIL | 3W1JG795YI | IACT |
| WITHANIA SOMNIFERA ROOT | V038D626IF | IACT |
| GLYCYRRHIZA GLABRA | 2788Z9758H | 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 |
|---|---|---|---|---|---|---|
| 5c008e11-ea31-6fbd-e053-2991aa0a951f | 5c008e11-ea30-6fbd-e053-2991aa0a951f | 2017-10-20 | Warnings | 5c008e11-ea31-6fbd-e053-2991aa0a951f 5c008e11-ea30-6fbd-e053-2991aa0a951f |
Adverse event summaries are temporarily unavailable. Other product information remains available.