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Over-the-counter medicine · no prescription needed

Octinoxate, oxybenzone and titanium dioxide

Purpose on the label: Sunscreen

Sunscreens

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

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.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Octinoxate, oxybenzone and titanium dioxide used for?
The Drug Facts label of Gr Bb Spf 25 (Erkul Kozmetik Sanayi Ve Ticaret Anonim Sirketi) lists these 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.
Do I need a prescription for Octinoxate, oxybenzone 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 Octinoxate, oxybenzone 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.

Gr Bb Spf 25 · Erkul Kozmetik Sanayi Ve Ticaret Anonim Sirketi

Octinoxate 2.5% · Oxybenzone 0.25% · Titanium dioxide 4.95%, cream (topical)

Active ingredient

Octinoxate 2.5% w/v Oxybenzone 0.25% w/v Titanium Dioxide 4.95% w/v

Purpose

Sunscreen

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

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.

Stop use and ask a doctor if

  • rash occurs

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • apply generously 15 minutes before the sun exposure
  • apply to cleansed skin
  • can be applied two coats to increase coverage
  • 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 sun Broad Spectrum SPF value of 15 or higher and other protection measures including:
  • limit time in the sun, especially from 10 a.m. - 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses.
  • children under 6 months of age: Ask a doctor

Inactive ingredients

Water (Aqua), Cyclopentasiloxane, Isododecane, Glycerin, PEG-9 Polydimethylsiloxyethyl Dimethicone, Butylene Glycol, Phenyl Trimethicone, Talc, Acrylates/Dimethicone Copolymer, Silica Dimethyl Silylate, Sodium Chloride, Phenoxyethanol, Disteardimonium Hectorite, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone, Tocopheryl Acetate, PEG/PPG-18 /18 Dimethicone, White Bird of Paradise (Strelitzia nicolai) Seed Aril Extract, Propylene Carbonate, Pentylene Glycol, Potassium Sorbate, Disodium EDTA, Sorbic Acid, Triethoxycaprylylsilane, Lactic Acid, Serine, Sodium Lactate, Sorbitol, Urea, Magnesium Stearate, Fragrance, Silica, Isoceteth-10, Aluminum Hydroxide, Allantoin, Linalool, Mica*, Iron Oxides*, Bismuth Oxychloride*. * contains one or more of these ingredients

— FDA label of Gr Bb Spf 25, Erkul Kozmetik Sanayi Ve Ticaret Anonim Sirketi, effective August 6, 2025. See the official label on DailyMed →

WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20 · Skinmetics Inc

Octinoxate 60 mg/mL · Oxybenzone 30 mg/mL · Titanium dioxide 30 mg/mL, cream (topical)

Active ingredient

Octinoxate 6% Oxybenzone 3% Titanium Dioxide 3% Purpose Sunscreen

Purpose

Sunscreen

Uses

helps prevent sunburn if used as directed with other sun protection measures (see ), decreases the risk of skin cancer and early skin aging caused by the sun. Directions

Warnings

For external use only Do not ues on damaged or broken skin

When using this product

keep out of the eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs.

Keep out of reach of children

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating. immediately after swimming or sweating immediately after towel drying at least every 2 hours 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 of 15 or higher and other sun protection measures including: Sun Protection Measures. limit time in the sun, especially from 10 a.m. 0 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses children under 6 months: Ask a doctor reapply:

Inactive ingredients

Aqua (Deionized Water), Dioctyl Maleate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Propylene Glycol, Camellia Sinensis (Green Tea) Leaf Extract, Marine Native Collagen Fluid, Retinyl Palmitate, Tocopherol Acetate, Persea Gratissima (Avocado) Oil, Daucus Carota Sativa (Carrot) Seed Oil, Matricaria Recutita (Chamomile) Flower Extract

Questions?

Call toll free 1-800-440-3032 or visit www.wilmaschumann.com

— FDA label of WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20, Skinmetics Inc, effective November 11, 2023. 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.

Octinoxate 2.5% · Oxybenzone 0.25% · Titanium dioxide 4.95% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Gr Bb Spf 25 Erkul Kozmetik Sanayi Ve Ticaret Anonim Sirketi DailyMed
Octinoxate 60 mg/mL · Oxybenzone 30 mg/mL · Titanium dioxide 30 mg/mL · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20 Skinmetics Inc DailyMed

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.

  • Erkul Kozmetik Sanayi Ve Ticaret Anonim Sirketi1 product
  • Skinmetics Inc1 product

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Next steps

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. 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.

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