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 and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating, immediately after toweling drying and at least every 2 hours children under 6 months of age: 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 with a Br...
Zinc Oxide 15.2%
Sunscreen
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
protect this product in this container from excessive heat and direct sun.
Water/Aqua/Eau, Butyloctyl Salicylate, Isodecyl Neopentanoate, Calcium Sodium Borosilicate, Diheptyl Succinate, C18-21 Alkane, Erythritol, Cetearly Alcohol, Sodium Stearoyl Glutamate, Capryloyl Glycerin/Sebacic Acid Copolymer, Propanediol, Archidyl Alcohol, Glycerin, Pyrus Malus (Apple) Fruit Extract, Caprylic/Capric Triglyceride, Tocopherol, Caprylyl Glycol, Coco-Glucoside, Ethyl Ferulate, Behenyl Alcohol, Cetyl Alcohol, Archidyl Glucoside, Bisabolol, Polyhydroxystearic Acid, Citric Acid, Sodium Gluconate, Xanthan Gum, Octyldodecyl Oleate, Caprylhydroxamic Acid, Hydrolyzed Jojoba Esters, Sodium Hyaluronate, Crithmum Maritimum Extract, Maltodextrin, Moringa Oleifera Seed Extract, Aloe Barbadensis Leaf, Iron Oxides (CI 77491, CI 77492).
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 73690-025 | 73690-025-01 |
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 |
|---|---|---|---|---|---|---|
| f200f199-23f1-e140-e053-2995a90aeffd | a35a232f-7e7b-5237-e053-2a95a90a8986 | 2023-01-11 | Warnings | a35a232f-7e7b-5237-e053-2a95a90a8986 |
Adverse event summaries are temporarily unavailable. Other product information remains available.