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Over-the-counter medicine · no prescription needed

Octinoxate, octisalate, oxybenzone and titanium dioxide

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 Octinoxate, octisalate, oxybenzone and titanium dioxide used for?
The Drug Facts label of COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR (Bluemercury) 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 Octinoxate, octisalate, oxybenzone 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 Octinoxate, octisalate, oxybenzone 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.

COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR · Bluemercury

Octinoxate 7.5% · Octisalate 5% · Oxybenzone 3% · Titanium dioxide 6.74%, cream (topical)

Active ingredient

Purpose Octinoxate 7.5% sunscreen Octisalate 5% sunscreen Oxybenzone 3% sunscreen Titanium Dioxide 6.74% sunscreen

Purpose

Active Ingredients Purpose Octinoxate 7.5% sunscreen Octisalate 5% sunscreen Oxybenzone 3% sunscreen Titanium Dioxide 6.74% 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. Reapply at least every 2 hours. Use a water resistant sunscreen if 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 of 15 or higher and other sun protection measure including: Limit time in the sun, especially from 10am - 2pm. Wear long-sleeve shirts, pants, hats and sunglasses. Children under 6 months of age: Ask a doctor.

Inactive ingredients

Water (Aqua), Phenyl Trimethicone, Neopentyl Glycol Dicaprate, Butylene Glycol, Glycerin, C20-40 Pareth-3, Caprylyl Methicone, Steareth-21, Glycereth-26, Dipropylene Glycol, PEG-8 Dimethicone, Silica, Tocopheryl Acetate, Sodium Hyaluronate, Citrus Aurantium Amara (Bitter Orange) Peel Oil, Dimethicone, Phenoxyethanol, Potassium Cetyl Phosphate, Stearyl Alcohol, Trimethylsiloxysilicate, Caprylyl Glycol, Mica, PEG-32, Polypropylsilsesquioxane, VP/Eicosene Copolymer, Polyethylene, Hydroxyethyl Acrylate/Sodium Accryloyldimethyl Taurate Copolymer, Hydrolyzed Wheat Protein/PVP Crosspolymer, Sorbitol, Decylene Glycol, Isohexadecane, Steareth-21, Cellulose Gum, Allantoin, Dipotassium Glycyrrhizate, Disodium EDTA, Polysorbate 60, Adenosine, Aminomethyl Propanol, Aminoethylphosphinic Acid, Hippophae Rhamnoides oil, Palmaria Palmata Extract, Cichorium Intybus (Chicory) Root Extract, Ethylhexylglycerin, Lecithin, Ammonium Polyacrylate, Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499), Titanium Dioxide (CI 77891)

— FDA label of COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR, Bluemercury, effective January 29, 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.

Octinoxate 7.5% · Octisalate 5% · Oxybenzone 3% · Titanium dioxide 6.74% · cream (topical) · 6 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR Bluemercury DailyMed
COVER plus CORRECT/TINTED MOISTURIZER CC CRM GOLDEN LIGHT Bluemercury DailyMed
COVER plus CORRECT/TINTED MOISTURIZER CC CRM LIGHT Bluemercury DailyMed
COVER plus CORRECT/TINTED MOISTURIZER CC CRM MED Bluemercury DailyMed
COVER plus CORRECT/TINTED MOISTURIZER CC CRM MED/DEEP Bluemercury DailyMed
COVER plus CORRECT/TINTED MOISTURIZER CC CRM PORCELAIN Bluemercury 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.

  • Bluemercury6 products

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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