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Over-the-counter medicine · no prescription needed

Homosalate, octisalate, octocrylene 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 Homosalate, octisalate, octocrylene and titanium dioxide used for?
The Drug Facts label of Jmsolution Skin Boost Niacinamide Sunscreen (Gpny Corp) 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 Homosalate, 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 Homosalate, 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.

Jmsolution Skin Boost Niacinamide Sunscreen · Gpny Corp

Homosalate 6.3 g/50 mL · Octisalate 2.5 g/50 mL · Octocrylene 4.35 g/50 mL · Titanium dioxide 0.9 g/50 mL, cream (topical)

Active ingredient

Homosalate 12.6 % Octisalate 5.0 % Octocrylene 8.7 % Titanium Dioxide 1.8 %

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 skin aging caused by the sun

Warnings

For external use only

Do not use

  • on damaged skin 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 liberally 15 minutes before sun exposure 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 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
  • reapply at least every 2 hours
  • use a water-resistant sunscreen if swimming or sweating

Other information

  • protect the product from excessive heat and direct sun
  • Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive ingredients

Water, Butyloctyl Salicylate, Polymethylsilsesquioxane, Cetearyl Glucoside, Benzyl Glycol, Glyceryl Stearate SE, Sorbitan Olivate, Poly C10-30 Alkyl Acrylate, Arginine, Butylene Glycol, Silica, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Polysorbate 60, Oleth-10, 1,2-Hexanediol, Dimethicone, Panthenol, Cetearyl Alcohol, Xanthan Gum, Hydroxypropyl Methylcellulose Stearoxy Ether, Ethylhexylglycerin, Glutathione, Niacinamide, Ceramide NP, Zinc PCA, Tocopherol, Glyceryl Glucoside, Glycerin, Sodium Hyaluronate, Centella Asiatica Extract, Fragrance, Linalool, Limonene

— FDA label of Jmsolution Skin Boost Niacinamide Sunscreen, Gpny Corp, effective April 29, 2026. See the official label on DailyMed →

Bombee Honey Daily Glow Shield Sunscreen · ABT ASIA Inc.

Homosalate 3.65 g/50 mL · Octisalate 2.45 g/50 mL · Octocrylene 4.9 g/50 mL · Titanium dioxide 0.9 g/50 mL, cream (topical)

Active ingredient

Homosalate 7.3% Octisalate 4.9% Octocrylene 9.8% Titanium Dioxide 1.8%

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 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 liberally 15 minutes before sun exposure. 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 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
  • reapply at least every 2 hours
  • use a water-resistant sunscreen if swimming or sweating

Other information

  • protect the product from excessive heat and direct sun
  • Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive ingredients

Water, Butyloctyl Salicylate, Dicaprylyl Carbonate, Niacinamide, Polysorbate 80, Glyceryl Stearate, PEG-100 Stearate, Pentylene Glycol, Glyceryl Stearate SE, Ethylhexyl Methoxycrylene, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Poly C10-30 Alkyl Acrylate, Butylene Glycol, Phenyl Trimethicone, Silica, Honey Extract, Diphenyl Dimethicone, Polysorbate 60, Oleth-10, Polyacrylate Crosspolymer-6, 1,2-Hexanediol, Dimethicone, Methylpropanediol, Royal Jelly Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxypropyl Methylcellulose Stearoxy Ether, Propolis Extract, Potassium Cetyl Phosphate, Tromethamine, Panthenol, Xanthan Gum, Caprylyl Glycol, Ethylhexylglycerin, Adenosine, Sodium Polyphosphate, Glycerin, Curcumin, Steareth-30, Ascorbic Acid, Tocopherol, Hydrogenated Lecithin, Caprylic/Capric Triglyceride, Dipropylene Glycol, Cetearyl Olivate, Sorbitan Olivate, Polyglyceryl-3 Methylglucose Distearate, Sodium Hyaluronate, Rumex Crispus Root Extract, Inula Britannica Flower Extract, Rose Extract, Camellia Sinensis Leaf Extract, Ceramide NP, Cetearyl Alcohol, Cholesterol, Ascorbyl Propyl Hyaluronate, Sodium DNA, Ascorbic Acid Polypeptide, Sodium Ascorbyl Phosphate, Phytosphingosine, Folic Acid, Magnesium Ascorbyl Phosphate, Tetrahexyldecyl Ascorbate, Sodium Riboflavin Phosphate, Thiamine HCl, Riboflavin, Pyridoxine, Ascorbyl Glucoside, Biotin, Cyanocobalamin, Fragrance, Linalool, Limonen

— FDA label of Bombee Honey Daily Glow Shield Sunscreen, ABT ASIA Inc., effective July 8, 2026. See the official label on DailyMed →

Sun Does Matter Daily Face Sunscreen · Sundoesmatter Company Inc.

Homosalate 3.65 g/50 mL · Octisalate 4.9 g/50 mL · Octocrylene 2.45 g/50 mL · Titanium dioxide 0.9 g/50 mL, cream (topical)

Active ingredient

Homosalate 7.3% Octisalate 4.9% Octocrylene 9.8% Titanium Dioxide 1.8%

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 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 liberally 15 minutes before sun exposure. 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 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
  • reapply at least every 2 hours
  • use a water-resistant sunscreen if swimming or sweating

Other information

  • protect the product from excessive heat and direct sun
  • Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive ingredients

Water, Butyloctyl Salicylate, Dicaprylyl Carbonate, Niacinamide, Polysorbate 80, Glyceryl Stearate, PEG-100 Stearate, Pentylene Glycol, Glyceryl Stearate SE, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Ethylhexyl Methoxycrylene, Butylene Glycol, Poly C10-30 Alkyl Acrylate, Phenyl Trimethicone, Silica, Polysorbate 60, Polyacrylate Crosspolymer-6, Oleth-10, Diphenyl Dimethicone, Fragrance, 1,2-Hexanediol, Dimethicone, Methylpropanediol, Potassium Cetyl Phosphate, Panthenol, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxypropyl Methylcellulose Stearoxy Ether, Xanthan Gum, Glycerin, Adenosine, Ethylhexylglycerin, Caprylyl Glycol, Sodium Polyphosphate, Limonene, Tocopherol, Ectoin, Rumex Crispus Root Extract, Camellia Sinensis Leaf Extract, Inula Britannica Flower Extract, Polyglyceryl-10 Oleate, Caryodendron Orinocense Seed Oil, Plukenetia Volubilis Seed Oil, Linalool, Curcumin, Bacillus/Folic Acid/Soybean Ferment Extract, Steareth-30, Butyrospermum Parkii (Shea) Butter, Hydrogenated Lecithin, Bakuchiol, Sodium Hyaluronate, Aloe Ferox Leaf Extract, Thymus Vulgaris (Thyme) Extract

— FDA label of Sun Does Matter Daily Face Sunscreen, Sundoesmatter Company Inc., effective June 27, 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.

Homosalate 6.3 g/50 mL · Octisalate 2.5 g/50 mL · Octocrylene 4.35 g/50 mL · Titanium dioxide 0.9 g/50 mL · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Jmsolution Skin Boost Niacinamide Sunscreen Gpny Corp DailyMed
Homosalate 3.65 g/50 mL · Octisalate 2.45 g/50 mL · Octocrylene 4.9 g/50 mL · Titanium dioxide 0.9 g/50 mL · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Bombee Honey Daily Glow Shield Sunscreen ABT ASIA Inc. DailyMed
Homosalate 3.65 g/50 mL · Octisalate 4.9 g/50 mL · Octocrylene 2.45 g/50 mL · Titanium dioxide 0.9 g/50 mL · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Sun Does Matter Daily Face Sunscreen Sundoesmatter Company 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.

  • Gpny Corp1 product
  • ABT ASIA Inc.1 product
  • Sundoesmatter Company Inc.1 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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