Quick answers
- What is Padimate o and titanium dioxide used for?
- The Drug Facts label of Vertra Pearl White Face Stick SPF 50 (Toshiki Pigment Co., Ltd.) lists these uses: Stop use and ask a doctor if: Rash or irritation develops and lasts.
- Do I need a prescription for Padimate o and titanium dioxide?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Padimate o and titanium dioxide been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Vertra Pearl White Face Stick SPF 50 · Toshiki Pigment Co., Ltd.
Padimate o 7% · Titanium dioxide 17%, stick (topical)
Active ingredient
Purpose PADIMATE O 7% Sunscreen TITANIUM DIOXIDE 17% Sunscreen
Purpose
Uses Helps prevent sunburn If used as directed with other sun protection (see directions), decreases the risk of skin cancer and early skin aging caused by the sun. Higher SPF gives more sunburn protection Retains SPF after 80 minutes activity in the water, sweating, or perspiring. Provides high protection against sunburn
Uses
Stop use and ask a doctor if: Rash or irritation develops and lasts
Warnings
Do not use
On damaged or broken skin
When using this product
keep out of eyes. Rinse with water to remove For external use only
Keep out of reach of children
: If product is swallowed get medical help or contact a Poison Control Center right away
Directions
Apply liberally and generously 15 minutes before sun exposure 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 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 Reapply: After 80 minutes of swimming or sweating Immediately after towel drying at least every 2 hours
Inactive ingredients
Hexyldecyl Isostearate, Mica, Synthetic Wax, Paraffin, Ozokerite, Polyglyceryl-2 Oleate, Aluminum Hydroxide, Stearic Acid, Ethylene/Propylene Copolymer, Tocopherol, Fragrance
— FDA label of Vertra Pearl White Face Stick SPF 50, Toshiki Pigment Co., Ltd., effective November 4, 2025. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Padimate o 7% · Titanium dioxide 17% · stick (topical) · 2 products
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Toshiki Pigment Co., Ltd.1 product
- Eai-jr 286, Inc1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.