Quick answers
- What is Ensulizole and titanium dioxide used for?
- The Drug Facts label of OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige (LG H&H Co., Ltd.) lists these uses: helps prevent sunburn if used as directed with other sun protection measures (see Directions ), may decrease the risk of skin cancer and early skin aging caused by the sun.
- Do I need a prescription for Ensulizole 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 Ensulizole 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.
OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige · LG H&H Co., Ltd.
Ensulizole 0.405 g/15 g · Titanium dioxide 0.819 g/15 g, powder (topical)
Active ingredient
ENSULIZOLE 2.7%, TITANIUM DIOXIDE 5.46%
Purpose
Sunscreen
Uses
helps prevent sunburn if used as directed with other sun protection measures (see Directions ), may decrease the risk of skin cancer and early skin aging caused by the sun
Warnings
For external use only
Do not use
Do not use
on damaged or broken skin When using
When using this product
. Keep out of the eyes. Rinse with water to remove. Stop use
Stop use and ask a 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 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, regulary 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.
Other information
protect this product from excessive heat and direct sun
Inactive ingredients
WATER, TRIETHYLHEXANOIN, DIMETHICONE, PHENYL TRIMETHICONE, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, CYCLOPENTASILOXANE, DIPENTAERYTHRITYL HEXA C5-9 ACID ESTERS, CETYL PEG/PPG-10/1 DIMETHICONE, NIACINAMIDE, TROMETHAMINE, 1,2-HEXANEDIOL, SORBITAN SESQUIOLEATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PEG-30 DIPOLYHYDROXYSTEARATE, SODIUM CHLORIDE, ZINC STEARATE, DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER, DISTEARDIMONIUM HECTORITE, ALUMINUM HYDROXIDE, STEARIC ACID, DISTEARYLDIMONIUM CHLORIDE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE, PALMITOYL PROLINE, PHENOXYETHANOL, ADENOSINE, BIOSACCHARIDE GUM-1, TRIETHOXYCAPRYLYLSILANE, MAGNESIUM PALMITOYL GLUTAMATE, SODIUM PALMITOYL SARCOSINATE, PALMITIC ACID, DIPROPYLENE GLYCOL, LUFFA CYLINDRICA FRUIT EXTRACT, HEXYL LAURATE, POLYGLYCERYL-4 ISOSTEARATE, SODIUM CITRATE, TOCOPHEROL, FRAGRANCE, TITANIUM DIOXIDE(CI 77891), MICA, IRON OXIDES(CI 77491, CI 77492, CI 77499)
Questions?
1-866-993-4709
— FDA label of OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige, LG H&H Co., Ltd., effective July 2, 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.
Ensulizole 0.405 g/15 g · Titanium dioxide 0.819 g/15 g · powder (topical) · 12 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| OHUI Ultimate Cover CC Cushion Compact 01 Light Beige | fmg Co.Ltd | DailyMed |
| OHUI Ultimate Cover CC Cushion Compact 01 Light Beige | LG H&H Co., Ltd. | DailyMed |
| OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige | fmg Co.Ltd | DailyMed |
| OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige | LG H&H Co., Ltd. | DailyMed |
| THEFACESHOP Cushion CC SPF 50 Apricot Beige Oil-Free | fmg Co.Ltd | DailyMed |
| THEFACESHOP Cushion CC SPF 50 Apricot Beige Oil-Free | LG H&H Co., Ltd. | DailyMed |
| THEFACESHOP Cushion CC SPF 50 Natural Beige Oil-Free | fmg Co.Ltd | DailyMed |
| THEFACESHOP Cushion CC SPF 50 Natural Beige Oil-Free | LG H&H Co., Ltd. | DailyMed |
| THEFACESHOP Cushion CC Total Cover SPF 50 Apricot Beige | fmg Co.Ltd | DailyMed |
| THEFACESHOP Cushion CC Total Cover SPF 50 Apricot Beige | LG H&H Co., Ltd. | DailyMed |
| THEFACESHOP Cushion CC Total Cover SPF 50 Natural Beige | fmg Co.Ltd | DailyMed |
| THEFACESHOP Cushion CC Total Cover SPF 50 Natural Beige | LG H&H 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.
- LG H&H Co., Ltd.6 products
- fmg Co.Ltd6 products
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.