OTC - ACTIVE INGREDIENT SECTION
Active Ingredient Purpose
Titanium Dioxide 10% Sunscreen
Zinc Oxide 12% Sunscreen
Active Ingredient Purpose
Titanium Dioxide 10% Sunscreen
Zinc Oxide 12% Sunscreen
Uses
Keep out of reach of children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Stop use and ask a doctor if rash occurs
Warnings
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.
Directions
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 including: • limit your time in the sun, especially from 10
a.m. – 2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses
Inactive Ingredients
Aqua (Deionized water), Ascorbyl Palmitate, Butyloctyl Salicylate, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Capryl/Caprylyl Glucoside, Chamomilla Recutita (Chamomile) Extract, Cocos Nucifera (Coconut) Oil, Daucus Carota Sativa (Carrot) Extract, Glycerin, Glyceryl Caprylate, Glyceryl Stearate Citrate, Glyceryl Undecylenate, Helianthus Annuus (Sunflower) Oil, Mangifera Indica (Mango) Butter, Polyhydroxystearic Acid, Punica Granatum (Pomegranate) Extract, Stearic Acid, Tocopherol (Vitamin E), Xanthan Gum, Zemea (Corn) Propanediol.
Supergoop
Sunnyscreen SPF 50 spray for babies + kiddos
Broad Spectrum Sunscreen SPF 50
Water Resistant (80 minutes)
3.4 fl oz./100 ml
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75936-252-01 | Sunnyscreen SPF 50 | 100 mL in 1 BOTTLE, SPRAY | SPRAY | 100 | 4 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 75936-252 | 75936-252-01 |
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 |
|---|---|---|---|---|---|---|
| 296576e5-df1e-5643-e063-6394a90a78c0 | 859461ea-582e-8185-e053-2991aa0a954a | 2024-12-16 | Warnings | 296576e5-df1e-5643-e063-6394a90a78c0 859461ea-582e-8185-e053-2991aa0a954a |
Adverse event summaries are temporarily unavailable. Other product information remains available.