Quick answers
- What is Ensulizole, octinoxate, oxybenzone, titanium dioxide and zinc oxide used for?
- The Drug Facts label of Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light (Access Business Group LLC) lists these uses: Helps prevent sunburn.
- Do I need a prescription for Ensulizole, octinoxate, oxybenzone, 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, oxybenzone, 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.
Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light · Access Business Group LLC
Ensulizole 20 mg/mL · Octinoxate 55 mg/mL · Oxybenzone 5 mg/mL · Titanium dioxide 8.8 mg/mL · Zinc oxide 98 mg/mL, cream (topical)
Active ingredient
Ensulizole 2.0% (W/W P/P) Octinoxate 5.5% (W/W P/P) Oxybenzone 0.5% (WW P/P) Titanium Dioxide 0.84% (W/W P/P) Zinc Oxide 9.8% (W/W P/P) Purpose Sunscreen
Purpose
Sunscreen
Uses
- Helps prevent sunburn
Warnings
For external use only
Do not use
on broken or damaged skin
When using this product
keep out of eyes. Rinse with water to remove.
Keep out of reach of children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
For suncreen use
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating or washing
- Reapply at least every 2 hours
- 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 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-sleeve shirts, pants, hats, and sunglasses Sun Protection Measures.
Inactive ingredients
WATER/EAU/AQUA, DIMETHICONE, CYCLOPENTASILOXANE, METHYL TRIMETHICONE, BUTYLENE GLYCOL, GLYCERIN, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TALC, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE, TRIETHANOLAMINE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, POLYGLYCERYL-6 POLYRICINOLEATE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, PEG/PPG-18/18 DIMETHICONE, ALUMINA, POLYGLYCERYL-3, POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRISILOXANE, HYDROGEN DIMETHICONE, ALUMINUM HYDROXIDE, STEARIC ACID, TRIETHOXYCAPRYLYLSILANE, METHYLPARABEN, DISODIUM EDTA, FRAGRANCE/PARFUM, SILICA, PROPYLPARABEN, BELLIS PERENNIS (DAISY) FLOWER EXTRACT, MALTODEXTRIN, ETHYLPARABEN,, IODOPROPYNYL BUTYLCARBAMATE, JASMINUM OFFICINALE (JASMINE) FLOWER EXTRACT, LECITHIN, SOPHORA JAPONICA FLOWER POWDER, GERANIUM ROBERTIANUM EXTRACT, OENOTHERA BIENNIS (EVENING PRIMROSE) SEED EXTRACT, LACTOBACILLUS/ACEROLA CHERRY FERMENT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, HYDROLYZED CONCHIOLIN PROTEIN, TOCOPHERYL ACETATE, CERAMIDE-3, BETA-SITOSTEROL, TETRAHEXYLDECYL ASCORBATE, MAY CONTAIN/PEUT CONTEINIR: IRON OXIDES (CI 77491, CI 77492, CI 77499), MICA (CI 77019), TITANIUM DIOXIDE (CI 77891).
— FDA label of Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light, Access Business Group LLC, effective October 21, 2023. See the official label on DailyMed →
Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Deep · Amway Corp
Ensulizole 20 mg/mL · Octinoxate 55 mg/mL · Oxybenzone 5 mg/mL · Titanium dioxide 84 mg/mL · Zinc oxide 98 mg/mL, cream (topical)
Active ingredient
Ensulizole 2.0% (W/W P/P) Octinoxate 5.5% (W/W P/P) Oxybenzone 0.5% (WW P/P) Titanium Dioxide 0.84% (W/W P/P) Zinc Oxide 9.8% (W/W P/P) Purpose Sunscreen
Purpose
Sunscreen
Uses
Helps prevent sunburn
Warnings
For external use only
Do not use
on broken or damaged skin
When using this product
keep out of eyes. Rinse with water to remove.
Keep out of reach of children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
For suncreen use Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating or washing Reapply at least every 2 hours 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 of 15 or higher and other sun protection measures including: Sun Protection Measures. limit time in the sun, especially from 10 a.m. – 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses Children under 6 months: ask a doctor
Inactive ingredients
WATER/EAU/AQUA, DIMETHICONE, CYCLOPENTASILOXANE, METHYL TRIMETHICONE, BUTYLENE GLYCOL, GLYCERIN, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TALC, DIMETHICONE/ VINYL DIMETHICONE CROSSPOLYMER, TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE, TRIETHANOLAMINE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, POLYGLYCERYL-6 POLYRICINOLEATE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, PEG/PPG-18/18 DIMETHICONE, ALUMINA, POLYGLYCERYL-3, POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRISILOXANE, HYDROGEN DIMETHICONE, ALUMINUM HYDROXIDE, STEARIC ACID, TRIETHOXYCAPRYLYLSILANE, METHYLPARABEN, DISODIUM EDTA, FRAGRANCE/PARFUM, SILICA, PROPYLPARABEN, BELLIS PERENNIS (DAISY) FLOWER EXTRACT, MALTODEXTRIN, ETHYLPARABEN,, IODOPROPYNYL BUTYLCARBAMATE, JASMINUM OFFICINALE (JASMINE) FLOWER EXTRACT, LECITHIN, SOPHORA JAPONICA FLOWER POWDER, GERANIUM ROBERTIANUM EXTRACT, OENOTHERA BIENNIS (EVENING PRIMROSE) SEED EXTRACT, LACTOBACILLUS/ACEROLA CHERRY FERMENT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, HYDROLYZED CONCHIOLIN PROTEIN, TOCOPHERYL ACETATE, CERAMIDE-3, BETA-SITOSTEROL, TETRAHEXYLDECYL ASCORBATE, MAY CONTAIN/ PEUT CONTEINIR: IRON OXIDES (CI 77491, CI 77492, CI 77499), MICA (CI 77019), TITANIUM DIOXIDE (CI 77891).
— FDA label of Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Deep, Amway Corp, effective February 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.
Ensulizole 20 mg/mL · Octinoxate 55 mg/mL · Oxybenzone 5 mg/mL · Titanium dioxide 8.8 mg/mL · Zinc oxide 98 mg/mL · cream (topical) · 3 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium | Amway Corp | DailyMed |
| Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Medium | Amway Corp | DailyMed |
| Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light | Access Business Group LLC | DailyMed |
Ensulizole 20 mg/mL · Octinoxate 55 mg/mL · Oxybenzone 5 mg/mL · Titanium dioxide 84 mg/mL · Zinc oxide 98 mg/mL · cream (topical) · 2 products
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.
- Amway Corp4 products
- Access Business Group LLC1 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.