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Over-the-counter medicine · no prescription needed

Ethylhexyl methoxycinnamate 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 Ethylhexyl methoxycinnamate and titanium dioxide used for?
The Drug Facts label of MOOYAM Dark Skin Sunscreen (Guangdong Bisutang Biotechnology Co., Ltd) 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 aging caused by the sun.
Do I need a prescription for Ethylhexyl methoxycinnamate 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 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.

MOOYAM Dark Skin Sunscreen · Guangdong Bisutang Biotechnology Co., Ltd

Ethylhexyl methoxycinnamate 9.993% · Titanium dioxide 7.8%, cream (topical)

Active ingredient

ETHYLHEXYL METHOXYCINNAMATE ---9.993 TITANIUM DIOXIDE ----7.8

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 aging caused by the sun.

Warnings

Do not use

on damaged or broken skin. For external use only.

When using this product

keep out of eyes. If product gets into the eyes, rinse with water to remove Stop use and consult a doctor if rash occurs. KEEP OUT OF REACH OF CHILDREN

Directions

  • Apply generously and evenly to face and neck 15-20 minutes before sun exposure.
  • Reapply at least every 2 hours
  • Use a water-resistant sunscreen when swimming or sweating.
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early aging. To reduce this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: - Limiting time in the sun, especially from 10 a.m. - 2 p.m. - Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Children under 6 months: Ask a doctor.

Inactive ingredients

WATER PROPYLENE GLYCOL STEARIC ACID ETHYLHEXYL PALMITATE GLYCERIN GLYCERYL STEARATE PEG-100 STEARATE PHENOXYETHANOL CARAMEL POLYACRYLAMIDE C13-14 ISOPARAFFIN SORBITAN SESQUIOLEATE METHYLPARABEN LAURETH-7 FRAGRANCE BUTYLENE GLYCOL CI 19140 AKA102 L5630XRC87 SODIUM CHLORIDE ALUMINA CENTELLA ASIATICA EXTRACT POLYGONUM CUSPIDATUM ROOT EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT BHT CAMELLIA SINENSIS LEAF EXTRACT GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT CI 16035 CI 15985

— FDA label of MOOYAM Dark Skin Sunscreen, Guangdong Bisutang Biotechnology Co., Ltd, effective October 29, 2025. See the official label on DailyMed →

VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen · LCM TECHNOLOGY Co., Ltd

Ethylhexyl methoxycinnamate 7.5% · Titanium dioxide 1.35%, cream (topical)

Active ingredient

Ethylhexyl Methoxycinnamate (Octinoxate) 7.5% Titanium Dioxide (Nano) 1.35%

Purpose

sunscreen

Uses

Apply 15 minutes before sun exposure. Reapply at least every 2 hours. Children under 6 months of age: ask a doctor. Apply generously and evenly to face and exposed areas of the body.

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 using and consult a doctor if rash or irritation occurs.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and earlyskin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15or higher and other sun protection measures including:"limit time in the sun, especially from 10 a.m.-2 p.m.,wear long-sleeved shirts, pants, hats, and sunglasses

Directions

Helps prevent sunburn. Decreases the risk of skin cancer and early skin aging caused by the sun.

Inactive ingredients

Water, Ethylhexyl, Methoxycinnamate, Isododecane, Butylene Glycol, Cyclopentasiloxane, Niacinamide, Ethylhexyl, Salicylate, Silica, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Ethylhexyl Triazone, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ethylhexyl Dimethyl PABA, Bis-Ethylhexyloxypenol Methoxyphenyl Triazine, Potassium Cetyl Phosphate, Sodium Chloride, Diethylhexyl Carbonate, Butyloctyl Sulfate, Trimethylsiloxysilicate, Pentaerythrityl Tetraethylhexanoate, Glycerin, Squalane, Bisabolol, Sodium Chloride, Phenoxyethanol, Polysorbate, Sodium Benzoate.

— FDA label of VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen, LCM TECHNOLOGY Co., Ltd, effective August 7, 2026. See the official label on DailyMed →

Sunscreen · Mingyu (guangdong) Cosmetics Technology Co., Ltd

Ethylhexyl methoxycinnamate 7.5% · Titanium dioxide 4%, lotion (topical)

Active ingredient

ETHYLHEXYL METHOXYCINNAMATE 7.5% TITANIUM DIOXIDE(NANO) 4%

Purpose

Sun Protection

Uses

FUNCTION: Blocks UV rays. protects against sun damage, moisturizes and nourishes, feels light and breathable, and nourishes and beautifies the skin.

Warnings

PRECAUTIONS

Do not use

for food purposes.

Do not use

on broken skin; avoid contact with eyes. If product gets into eyes, rinse immediately with plenty of water. Discontinue use if discomfort occurs. Keep out of eyes: In case of contact with eyes, please fush thoroughly with water.

Directions

USAGE:For daytime use, apply an appropriate amount evenly to the face and body.

Inactive ingredients

WATER SACCHAROMYCES FERMENT FILTRATE DIPROPYLENE GLYCOL GLYCERIN C12-15 ALKYL BENZOATE CAPRYLYL METHICONE CYCLOPENTASILOXANE POLYMETHYLSILSESQUIOXANE METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL(NANO) BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE CYCLOHEXASILOXANE C20-22 ALKYL PHOSPHATE POTASSIUM CETYL PHOSPHATE HYDROXYACETOPHENONE SILICA C20-22 ALCOHOLS POLYGLYCERYL-10 MYRISTATE CETEARYL ALCOHOL POLYHYDROXYSTEARIC ACID TOCOPHERYL ACETATE CHLORPHENESIN DECYL GLUCOSIDE POLYACRYLATE CROSSPOLYMER-6 ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER POTASSIUM HYDROXIDE DISODIUM EDTA BISABOLOL DIMETHICONE ISOHEXADECANE POLYSORBATE 80 PROPYLENE GLYCOL SODIUM HYALURONATE CROSSPOLYMER SODIUM HYALURONATE SORBITAN OLEATE XANTHAN GUM PHENOXYETHANOL VIOLA YEDOENSIS EXTRACT PAEONIA LACTIFLORA ROOT EXTRACT TARAXACUM OFFICINALE (DANDELION) RHIZOME/ROOT EXTRACT CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT BHT 1,2-HEXANEDIOL LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT MALVA SYLVESTRIS (MALLOW) FLOWER EXTRACT HYDROLYZED SODIUM HYALURONATE SODIUM ACETYLATED HYALURONATE HYALURONIC ACID HYDROLYZED GLYCOSAMINOGLYCANS ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT ETHYLHEXYLGLYCERIN HYDROXYPROPYLTRIMONIUM HYALURONATE ALOE BARBADENSIS LEAF JUICE

— FDA label of Sunscreen, Mingyu (guangdong) Cosmetics Technology Co., Ltd, effective September 10, 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.

Ethylhexyl methoxycinnamate 9.993% · Titanium dioxide 7.8% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
MOOYAM Dark Skin Sunscreen Guangdong Bisutang Biotechnology Co., Ltd DailyMed
Ethylhexyl methoxycinnamate 7.5% · Titanium dioxide 1.35% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen LCM TECHNOLOGY Co., Ltd DailyMed
Ethylhexyl methoxycinnamate 7.5% · Titanium dioxide 4% · lotion (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Sunscreen Mingyu (guangdong) Cosmetics 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.

  • Guangdong Bisutang Biotechnology Co., Ltd1 product
  • LCM TECHNOLOGY Co., Ltd1 product
  • Mingyu (guangdong) Cosmetics Technology Co., Ltd1 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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