Quick answers
- What is Octinoxate, octisalate, octocrylene and titanium dioxide used for?
- The Drug Facts label of Sunscreen Emulsion SPF50plus (Guangzhou Senmai Biotechnology Co.) lists these uses: Helps prevent sunburn lf used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.
- Do I need a prescription for Octinoxate, octisalate, octocrylene 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, octisalate, octocrylene 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.
Sunscreen Emulsion SPF50plus · Guangzhou Senmai Biotechnology Co.
Octinoxate 3000 mg/30 mL · Octisalate 1500 mg/30 mL · Octocrylene 3000 mg/30 mL · Titanium dioxide 2400 mg/30 mL, lotion (topical)
Active ingredient
Octocrylene 10% Ethylhexyl Methoxycirnnamate 10% Titanium Dioxide 8% Ethylhexyl Salicylate 5%
Purpose
Sunscreen
Uses
Helps prevent sunburn lf used as directed with other sun protection measures, 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 and ask a doctor if rash occurs.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Conirol Center right away
Directions
Apply to face and neck, avoiding the eye area. Wait at least 30 minutes before sun exposure, or as directed by a physician. Reapply at least every 2 hours
Inactive ingredients
Water, Glycerin, Dicaprylyl Carbonate, Isononyllsononanoate, Caprylic/capric Triglyceride, Dimethicone, Ceryl PEG/PPG-10/1 Dimethicone, Butylene Glycol, Phenyl Trimethicone,Cyclopentasiloxane,Corn Gluten Amino Acids, Magnesium Stearate,Magnesium Sulfate,Tocopheryl Acetate, Quaternium-18Bentonite, Hydroxyacetophenone, 1,2-hexanediol, Aluminum Hydroxide, Stearic Acid, Disteardimonium Hectorite,Fragrance,Propylene Carbonate,BHT,Vitamin E
— FDA label of Sunscreen Emulsion SPF50plus, Guangzhou Senmai Biotechnology Co., effective January 8, 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.
Octinoxate 3000 mg/30 mL · Octisalate 1500 mg/30 mL · Octocrylene 3000 mg/30 mL · Titanium dioxide 2400 mg/30 mL · lotion (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.
- Guangzhou Senmai Biotechnology Co.1 product
- Guangzhou Senmai Biotechnology Co., Ltd.1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
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.