Quick answers
- What is Ethylhexyl methoxycinnamate, octocrylene and titanium dioxide used for?
- The Drug Facts label of Sunscreen SPF50 (Guangzhou Tinsun Biotechnology Company Limited) lists these uses: Block or absorb ultraviolet rays to preventskin from developing erythema, tanningand aging due to sun exposure.
- Do I need a prescription for Ethylhexyl methoxycinnamate, 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 Ethylhexyl methoxycinnamate, 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 SPF50 · Guangzhou Tinsun Biotechnology Company Limited
Ethylhexyl methoxycinnamate 6% · Octocrylene 4% · Titanium dioxide 2%, cream (topical)
Active ingredient
ETHYLHEXYL METHOXYCINNAMATE 6% OCTOCRYLENE 4% TITANIUM DIOXIDE 2%
Purpose
Sunscreen
Uses
Block or absorb ultraviolet rays to preventskin from developing erythema, tanningand aging due to sun exposure
Warnings
Do not use
on areas with skin abnormalitiessuch as wounds, swelling, or eczemd
Ask a doctor before use if
Photosensitivity skin diseases or taking certain photosensitivity medications
Stop use and ask a doctor if
Redness,itching, peeling, or stinging occurs after applying sunscreen KEEP OUT OF REACH OF CHILDREN SECTION
Directions
Take an appropriate amount of sunscreenon the palm of your hand and applyevenly to the face, neck, arms and otherareas exposed to the sun.
Inactive ingredients
WATER ISONONYL ISONONANOATE SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL LIMNANTHES ALBA (MEADOWFOAM) SEED OIL GLYCERIN BUTYLENE GLYCOL CYCLOPENTASILOXANE STEARETH-2 STEARETH-21 CAPRYLIC/CAPRIC TRIGLYCERIDE TOCOPHERYL ACETATE ALOE BARBADENSIS LEAF EXTRACT PORTULACA OLERACEA EXTRACT POLYSORBATE 80 RUTIN BETA-GLUCAN 1,2-HEXANEDIOL HYDROXYACETOPHENONE XANTHAN GUM ORYZANOL BISABOLOL SODIUM HYALURONATE ALLANTOIN DISODIUM EDTA AROMA
— FDA label of Sunscreen SPF50, Guangzhou Tinsun Biotechnology Company Limited, effective August 7, 2025. See the official label on DailyMed →
EELHOE Sunscreen · Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Ethylhexyl methoxycinnamate 2.5 mg/50 mg · Octocrylene 2.5 mg/50 mg · Titanium dioxide 0.05 mg/50 mg, lotion (topical)
Active ingredient
ETHYLHEXYL METHOXYCINNAMATE、OCTOCRYLENE、TITANIUM DIOXIDE
Purpose
1. Stop ultraviolet rays, reduce radiation, and lasting sunscreen. 2. Multiple isolation whitening isolation sunscreen, reducing the damage of makeup to the skin, and brightening the skin color. 3. Contains moisturizing ingredients, moisturize the skin while sunscreen, and make the skin soft and moist. 4. The texture is refreshing, not greasy, easy to absorb without blocking pores. 5. Mild ingredients, suitable for all skin types, including sensitive skin.
Uses
1. Take an appropriate amount of sunscreen at the end of your skin care routine. 2. Apply evenly to areas susceptible to UV radiation. 3. Wipe evenly.
Warnings
Please keep out of reach of children. Do not swallow. Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place. 1. Take an appropriate amount of sunscreen at the end of your skin care routine. 2. Apply evenly to areas susceptible to UV radiation. 3. Wipe evenly.
Directions
1. Take an appropriate amount of sunscreen at the end of your skin care routine. 2. Apply evenly to areas susceptible to UV radiation. 3. Wipe evenly.
Inactive ingredients
AQUA、ISONONYL ISONONANOATE、GLYCERYL STEARATE、ASCORBIC ACID
— FDA label of EELHOE Sunscreen, Shantou Eelhoe Daily Chemical Technology Co., Ltd., effective May 11, 2026. 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.
Ethylhexyl methoxycinnamate 6% · Octocrylene 4% · Titanium dioxide 2% · cream (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Sunscreen SPF50 | Guangzhou Tinsun Biotechnology Company Limited | DailyMed |
Ethylhexyl methoxycinnamate 2.5 mg/50 mg · Octocrylene 2.5 mg/50 mg · Titanium dioxide 0.05 mg/50 mg · lotion (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| EELHOE Sunscreen | Shantou Eelhoe Daily Chemical Technology Co., Ltd. | 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.
- Guangzhou Tinsun Biotechnology Company Limited1 product
- Shantou Eelhoe Daily Chemical Technology Co., Ltd.1 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.