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
For sunscreen use: shake well before use apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating 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 inclu...
protect the product in this container from excessive heat and direct sun
Octinoxate 7%
Sunscreen
For external use only
on damaged or broken skin
keep out of eyes. Rinse with water to remove.
rash occurs
If swallowed, get medical help or contact a Poison Control Center right away.
For sunscreen use:
water, cyclopentasiloxane, glycerin, dimethicone, PEG-10 dimethicone, sorbitol, bis-PEG/PPG-14/14 dimethicone, dimethicone/polyglycerin-3 crosspolymer, sodium chloride, phenoxyethanol, caprylyl glycol, disteardimonium hectorite, disodium stearoyl glutamate, ethylhexylglycerin, fragrance, aluminum hydroxide, ascorbyl palmitate, dipropylene glycol, isotridecyl isononanoate; may contain: titanium dioxide, iron oxides, bismuth oxychloride
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Octinoxate | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| Octinoxate | ACTIVE MOIETY | 4Y5P7MUD51 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 49967-064 | 49967-064-01, 49967-064-02, 49967-064-03 |
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 |
|---|---|---|---|---|---|---|
| 24f9c9fa-e0ad-419e-ba8b-e347e480ce08 | 0600c8a9-fcf7-4f1e-a6c2-4726fd159d1e | 2024-01-02 | Warnings | 24f9c9fa-e0ad-419e-ba8b-e347e480ce08 0600c8a9-fcf7-4f1e-a6c2-4726fd159d1e |
Adverse event summaries are temporarily unavailable. Other product information remains available.