■ apply generously and evenly 15 minutes before sun exposure ■ apply to all skin exposed to the sun ■ use a water resistant sunscreen if swimming or sweating ■ reapply at least every 2 hours ■ children under 6 months of age: Ask a doctor
Octinoxate 7.5%
Octisalate 5%
Oxybenzone 3%
Sunscreen
■ helps prevent sunburn.
Skin Cancer/Skin Aging Alert:Spending
time in the sun increases your risk of skin
cancer and early skin aging. This product has
been shown only to help prevent sunburn,
not
skin cancer or early skin aging.
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 a doctor ■ if rash occurs.
If product is
swallowed, get medical help or contact a
Poison Control Center right away.
■ apply generously and evenly 15 minutes
before sun exposure
■ apply to all skin exposed to the sun
■ use a water resistant sunscreen if
swimming or sweating
■ reapply at least every 2 hours
■ children under 6 months of age:
Ask a doctor
■ protect this product from excessive heat
and direct sun
■ may stain or damage some fabrics
or surfaces
water, octyldodecyl neopentanoate, glycerin,
emulsifying wax NF, glyceryl stearate,
PEG-100 stearate, dimethicone,
triethanolamine, diazolidinyl urea, carbomer,
methylparaben, ethylparaben, propylparaben,
bisabolol, farnesol, citric acid
Call 1-800-553-5340
PURPOSE ®
Dual
Treatment
Moisture
Lotion
Sunscreen
SPF 10
Oil-Free
Fragrance Free
Provides
Long-Lasting
Moisture
Developed with
Dermatologists
4 OZ (113g)
9474702
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 24208-001-04 | PURPOSE | 113 g in 1 BOTTLE | LOTION | 113 | 3 | |
| 24208-001-04 | PURPOSE | 1 in 1 CARTON | LOTION | 1 | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 24208-001 | 24208-001-04 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| OCTYLDODECYL NEOPENTANOATE | X8725R883T | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| GLYCERYL MONOSTEARATE | 230OU9XXE4 | IACT |
| PEG-100 STEARATE | YD01N1999R | IACT |
| DIMETHICONE | 92RU3N3Y1O | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| DIAZOLIDINYL UREA | H5RIZ3MPW4 | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| ETHYLPARABEN | 14255EXE39 | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| LEVOMENOL | 24WE03BX2T | IACT |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| OXYBENZONE | 95OOS7VE0Y | ACTIB |
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 |
|---|---|---|---|---|---|---|
| PURPOSE | OCTINOXATE, OCTISALATE AND OXYBENZONE | Bausch & Lomb Incorporated | a1e14135-b8da-4cee-8c5b-1893572f4de4 | 2024-09-25 | Warnings | 24208-001-04 24208-001 24208000104 22f5cdc2-86cc-7dfd-e063-6394a90a539d a1e14135-b8da-4cee-8c5b-1893572f4de4 |
Adverse event summaries are temporarily unavailable. Other product information remains available.