Active ingredient
Octinoxate 3%
Octinoxate 3%
aqua/water, cyclopentasiloxane, alcohol denat., butylene glycol, PEG-10 dimethicone, phenyl trimethicone, squalene, bis-PEG/PPG-14/14 dimethicone, magnesium sulfate, talc, nylon-12, maltitol, disodium stearoyl glutamate, aluminum hydroxide, sorbitol, perlite, vaccinium myrtillus fruit extract; may contain: ci 77891/titanium dioxide, ci 77491, ci 77492, ci 77499/iron oxides
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 49967-297 | 49967-297-01 |
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 |
|---|---|---|---|---|---|---|
| a9d9c954-d947-4d4a-a6a0-8eea68d9921d | 7ffd9560-574b-4bea-9fd1-59c07ead998f | 2024-01-30 | a9d9c954-d947-4d4a-a6a0-8eea68d9921d 7ffd9560-574b-4bea-9fd1-59c07ead998f |
Adverse event summaries are temporarily unavailable. Other product information remains available.