Quick answers
- What is Ensulizole, octinoxate, octisalate, titanium dioxide and zinc oxide used for?
- The Drug Facts label of THEFACESHOP Natural Sun Oil-Free Sunscreen Broad Spectrum SPF 50 (fmg 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 skin aging caused by the sun.
- Do I need a prescription for Ensulizole, octinoxate, octisalate, titanium dioxide and zinc oxide?
- 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 Ensulizole, octinoxate, octisalate, titanium dioxide and zinc oxide 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.
THEFACESHOP Natural Sun Oil-Free Sunscreen Broad Spectrum SPF 50 · fmg Co.Ltd
Ensulizole 1.75 g/50 mL · Octinoxate 3.5 g/50 mL · Octisalate 2.25 g/50 mL · Titanium dioxide 2.285 g/50 mL · Zinc oxide 5.825 g/50 mL, lotion (topical)
Active ingredient
Ensulizole 3.5% Octinoxate 7.00% Octisalate 4.5% Titanium Dioxide 4.57% Zinc Oxide 11.65%
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 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 and as needed. Reapply as needed or after towel drying, 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including: - Limit time in the sun, especially from 10 a.m. to 2 p.m. - Wear long-sleeved shirts, pants, hats, and sunglasses Children under 6 months: Ask a doctor
Inactive ingredients
WATER, CYCLOPENTASILOXANE, DIPROPYLENE GLYCOL, GLYCERIN, DICAPRYLYL CARBONATE, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TROMETHAMINE, DIMETHICONE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PANTHENOL, DISTEARDIMONIUM HECTORITE, ALUMINUM HYDROXIDE, ZINC STEARATE, SORBITAN SESQUIOLEATE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, STEARIC ACID, GLYCERYL CAPRYLATE, HYDROGEN DIMETHICONE, DISTEARYLDIMONIUM CHLORIDE, ETHYLHEXYLGLYCERIN, TRIETHOXYCAPRYLYLSILANE, TRISODIUM EDTA, HELIANTHUS ANNUS (SUNFLOWER) SRPOUT EXTRACT, MENTHYL PCA, SODIUM PCA, SODIUM BENZOATE, TITANIUM DIOXIDE (CI 77891), FRAGRANCE
Questions?
Call toll free 1-888-498-9004
— FDA label of THEFACESHOP Natural Sun Oil-Free Sunscreen Broad Spectrum SPF 50, fmg Co.Ltd, effective January 1, 2025. See the official label on DailyMed →
Eucerin Daily Protection Face · Beiersdorf Inc
Ensulizole 2% · Octinoxate 7.5% · Octisalate 4.5% · Titanium dioxide 2.4% · Zinc oxide 4.8%, lotion (topical)
Active ingredient
Ensulizole 2% Octinoxate 7.5% Octisalate 4.5% Titanium Dioxide 2.4% Zinc Oxide 4.8%
Purpose
Sunscreens
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
irritation occurs
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
For sunscreen use:
- apply liberally 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
- 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
Inactive ingredients
Water, Glycerin, C12-15 Alkyl Benzoate, Dimethicone, Cyclomethicone, Methylpropanediol, Cetearyl Alcohol, Cetyl Alcohol, Ceteareth-20, Phenoxyethanol, Glyceryl Stearate SE, Sodium Lactate, Lactic Acid, 1,2-Hexanediol, Hydrogenated Coco-Glycerides, VP/Hexadecene Copolymer, Xanthan Gum, PEG-40 Castor Oil, Sodium Hydroxide, Trisodium EDTA, Alumina, Sodium Cetearyl Sulfate, Triethoxycaprylylsilane, Simethicone
Questions?
1-800-227-4703
— FDA label of Eucerin Daily Protection Face, Beiersdorf Inc, effective December 16, 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.
Ensulizole 1.75 g/50 mL · Octinoxate 3.5 g/50 mL · Octisalate 2.25 g/50 mL · Titanium dioxide 2.285 g/50 mL · Zinc oxide 5.825 g/50 mL · lotion (topical) · 6 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Babience KIDS Sunscreen pinkfong BABY SHARK SPF 50 | fmg Co.Ltd | DailyMed |
| Babience KIDS Sunscreen pinkfong BABY SHARK SPF 50 | LG H&H Co., Ltd. | DailyMed |
| THEFACESHOP Natural Sun Long Lasting Sunscreen Broad Spectrum SPF 50 | fmg Co.Ltd | DailyMed |
| THEFACESHOP Natural Sun Long Lasting Sunscreen Broad Spectrum SPF 50 | LG H&H Co., Ltd. | DailyMed |
| THEFACESHOP Natural Sun Oil-Free Sunscreen Broad Spectrum SPF 50 | fmg Co.Ltd | DailyMed |
| THEFACESHOP Natural Sun Oil-Free Sunscreen Broad Spectrum SPF 50 | LG H&H Co., Ltd. | DailyMed |
Ensulizole 2% · Octinoxate 7.5% · Octisalate 4.5% · Titanium dioxide 2.4% · Zinc oxide 4.8% · lotion (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Eucerin Daily Protection Face | Beiersdorf 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.
- fmg Co.Ltd3 products
- LG H&H Co., Ltd.3 products
- Beiersdorf Inc1 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.