OTC - PURPOSE SECTION
Sunscreen
Sunscreen
For external use only.
When using this product, keep out of eyes, rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply liberally 15 mintues before sun exposure. Use a water-resistant sunscreen if swimming or sweating:
Immediately after towel drying
At least every two hours
Children under 6 months: ask a doctor
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 rated SPF 15 or higher and other sun protection measures including:
Limit time in the sun, especially from 10 a.m. - 2 p.m.
Wear a long-sleeve shirt, pants, sunglasses, and a hat.
Protect this product from excessive heat and direct sun. Store at 20-25C (66-77F).
Water, Glycerin, Silica, Dimethicone, Benzyl Alcohol, Tocopherol, Chamomilla Recutita (Matricaria) Flower Extract, Vitis Vinifera (Grape) Seed Extract, Camellia Sinensis (Green Tea) Leaf Extract, Camellia Oleifera (Green Tea) Leaf Extract, Peucedanum Graveolens (Dill) Extract, Sambucus Nigra (Black Elderberry) Fruit Extract, Avena Sativa (Oat) Bran Extract, Punica Granatum (Pomegranate) Extract, Lycium Barbarum (Goji) Fruit Extract, Hydrogenated Lecithin, Titanium Dioxide, Dimethicone/Vinyl Dimethicone Crosspolymer, Diethylhexyl Syringylidenemalonate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Xanthan Gum, Sodium Carbomer, Sodium Benzoate, Potassium Sorbate, Phenoxyethanol
Avobenzone 2.0%
Octinoxate 7.5%
Octisalate 5.0%
Octocrylene 2.0%
• Dosage and Administration
1-21-2021
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 76144-613 | 76144-613-01, 76144-613-02 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| c54de183-3159-3b44-e053-2995a90a1deb | b96f9839-a5cd-b356-e053-2995a90aa8cf | 2022-01-06 | Warnings | c54de183-3159-3b44-e053-2995a90a1deb b96f9839-a5cd-b356-e053-2995a90aa8cf |
Adverse event summaries are temporarily unavailable. Other product information remains available.