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Over-the-counter medicine · no prescription needed

Homosalate, octinoxate, octisalate, octocrylene and zinc oxide

Purpose on the label: Section

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, octinoxate, octisalate, octocrylene and zinc oxide used for?
The Drug Facts label of X-Treme Cream Propolis Sunscreen SPF 45 (Epicuren Discovery) lists these uses: and Uses.
Do I need a prescription for Homosalate, octinoxate, octisalate, octocrylene 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 Homosalate, octinoxate, octisalate, octocrylene 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.

X-Treme Cream Propolis Sunscreen SPF 45 · Epicuren Discovery

Homosalate 8.5% · Octinoxate 7.5% · Octisalate 5% · Octocrylene 5% · Zinc oxide 4.5%, cream (topical)

Active ingredient

OTC Active Ingredient Section

Purpose

Section

Uses

and Uses

Warnings

Section Keep out of Reach of Children Section

Directions

Dosage

Other information

Other Safety Information

Inactive ingredients

section

— FDA label of X-Treme Cream Propolis Sunscreen SPF 45, Epicuren Discovery, effective July 14, 2026. See the official label on DailyMed →

CeraVe Facial Moisturizing with Sunscreen Broad Spectrum SPF 30 · LOreal USA Products Inc

Homosalate 100 mg/mL · Octinoxate 50 mg/mL · Octisalate 50 mg/mL · Octocrylene 20 mg/mL · Zinc oxide 80 mg/mL, lotion (topical)

Active ingredient

Homosalate 10% Octinoxate 5% Octisalate 5% Octocrylene 2% Zinc oxide 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

For sunscreen use: 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 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, niacinamide, cetearyl alcohol, glycerin, propanediol, dimethicone, behentrimonium methosulfate, BHT, ceramide NP, ceramide AP, ceramide EOP, carbomer, triethoxycaprylylsilane, triethyl citrate, sodium lauroyl lactylate, sodium hyaluronate, sodium phosphate, cholesterol, aluminum starch octenylsuccinate, phenoxyethanol, disodium phosphate, hydroxyethylcellulose, hydroxyacetophenone, caprylyl glycol, trisodium ethylenediamine disuccinate, phytosphingosine, xanthan gum, polysorbate 60, benzoic acid

Questions?

Toll-free number 1-888-768-2915

— FDA label of CeraVe Facial Moisturizing with Sunscreen Broad Spectrum SPF 30, LOreal USA Products Inc, effective March 27, 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.

Homosalate 8.5% · Octinoxate 7.5% · Octisalate 5% · Octocrylene 5% · Zinc oxide 4.5% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
X-Treme Cream Propolis Sunscreen SPF 45 Epicuren Discovery DailyMed
Homosalate 100 mg/mL · Octinoxate 50 mg/mL · Octisalate 50 mg/mL · Octocrylene 20 mg/mL · Zinc oxide 80 mg/mL · lotion (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
CeraVe Facial Moisturizing with Sunscreen Broad Spectrum SPF 30 LOreal USA Products 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.

  • Epicuren Discovery1 product
  • LOreal USA Products Inc1 product

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

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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