Coppertone Sport Sunscreen Lotion SPF 50 for oily acne-prone skin
Avobenzone
Homosalate
Octisalate
Octocrylene
Tocopherol Vitamin EAverage
- HighOily Skin Fit
- AverageEffectiveness
- HighSafety
Works for oily acne-prone skin; other sunscreens fit it better.
This fit is calculated for the concerns frequently associated with oily acne-prone skin: shine, breakouts, blemishes, and enlarged pores. For scores and recommendations based on your full skin profile, including your 12D face scan results and any goals or preferences you have, please use the Lovi app.
Page built Nov 8, 2026How the Fit score works
Lovi Assistant explains
- Offers moderate suitability for your oily skin, as Aluminum Octenylsuccinate Starch and Silica effectively absorb excess oil and provide a mattifying effect, though it lacks specialized ingredients like salicylic acid to target your acne and blemishes.
- The formula provides excellent UV protection with avobenzone, homosalate, octisalate, and octocrylene, which is beneficial for general skin health, but does not directly address your primary concerns.
- The safety profile is excellent, with no risks of irritation for your oily skin due to the absence of prohibited or harsh ingredients.
How to apply
- Apply this sunscreen AM as the final step of your morning skincare routine. Reapply every two hours when exposed to the sun for continuous protection.
- Apply after your moisturizer as the last step before makeup. Do not apply anything on top of your sunscreen.
- Gently spread a coin-sized amount evenly across your face and neck. Avoid harsh rubbing to prevent disturbing the protective layer.
- Apply on completely dry skin after your moisturizer has fully absorbed. This ensures the sunscreen forms an even, protective barrier.
- Avoid direct contact with your eyes during application. Do a patch test before first use to ensure no irritation occurs.
Questions and answers
How well does Coppertone Sport Sunscreen SPF 50 work for oily acne-prone skin?
Coppertone Sport Sunscreen SPF 50 works reasonably well for oily acne-prone skin, as it absorbs excess oil and protects against the sun without causing irritation, though it lacks specialized ingredients to actively target acne. To work best for this skin, a sunscreen of this type needs lightweight, oil-free ingredients and acne-fighting components like salicylic acid.
Journal of Drugs in Dermatology, 2025Archives of Dermatological Research, 2024
Which ingredients make this lotion a good fit for oily acne-prone skin?
Aluminum Octenylsuccinate Starch and silica make this lotion a decent fit by soaking up extra oil and keeping your skin looking matte. However, a product of this type needs specialized ingredients like salicylic acid to properly target your breakouts.
What does Avobenzone do for oily acne-prone skin?
Avobenzone helps protect your skin from sun damage, but it does not treat oily or acne-prone skin on its own. Sunscreens for this skin type need ingredients that feel light, absorb excess oil, and won't clog your pores.
What does Homosalate do for oily acne-prone skin?
Homosalate acts as a UV filter in sunscreen to protect oily and acne-prone skin from sun damage without feeling heavy. Chemical sunscreens containing this ingredient show a very low likelihood of causing skin irritation or breakouts.
Where does it go in a skincare routine for oily acne-prone skin?
This sunscreen goes as the last step of your morning skincare routine, right after your moisturizer. It is unlikely to irritate your skin, but an ideal product for oily acne-prone skin should also include targeted ingredients like salicylic acid to help clear breakouts.
Can I use this lotion with retinol, and in what order?
You can use this sunscreen in the morning as the final step of your skincare routine, after your moisturizer and before any makeup. It is safe for oily skin and unlikely to cause irritation, though it does not contain ingredients like salicylic acid to directly target breakouts.
How often should I use it?
Use this sunscreen every morning as the final step of your daytime routine. Chemical sunscreens containing avobenzone, octocrylene, homosalate, and octisalate are safe for daily use and are unlikely to cause skin irritation.
Can it clog pores, cause breakouts or purging for oily acne-prone skin?
This sunscreen is unlikely to irritate oily skin, but it lacks specialized acne-fighting ingredients like salicylic acid to target breakouts. For oily acne-prone skin, this type of product needs added blemish-targeting ingredients to fully address breakouts.
Journal of Drugs in Dermatology, 2025Archives of Dermatological Research, 2024
Is this lotion fragrance-free and alcohol-free?
Yes, it has no fragrance and no drying alcohol. Arachidyl alcohol and behenyl alcohol are fatty alcohols, which soften the skin.
What the research says
Chemical sunscreens containing avobenzone, octocrylene, homosalate, and octisalate showed no to minimal risks of dermal irritation, sensitization, photo-allergy, and photo-irritation in human subjects.
Journal of Drugs in Dermatology, 2025Incorporating rosmarinic acid into sunscreens enhanced the in vivo SPF of octocrylene by over 157% and reduced lipid peroxidation in the human stratum corneum.
Antioxidants, 2025Encapsulating avobenzone in low-porosity TiO2-embedded mesoporous silica (TiO2/SBA-S) reduced cutaneous avobenzone absorption from 0.76 to 0.50 nmol/mg while providing effective pollutant adsorbability, UVA protection, and a two- to three-fold reduction in photoaged skin cytokines/chemokines compared to the non-treatment control.
European Journal of Pharmaceutical Sciences, 2023The application of a sunscreen formulation containing ethylhexyl methoxycinnamate, ethylhexyl salicylate, methyl anthranilate, and octocrylene does not significantly affect critical acne-related species such as Cutibacterium acnes and Staphylococcus epidermidis, refuting the induction of facial dysbiosis in men.
Archives of Dermatological Research, 2024Encapsulation of ethylhexyl methoxycinnamate and butyl methoxydibenzoylmethane in lipid microparticles significantly reduced their in vivo human skin penetration compared to nonencapsulated filters.
Skin Pharmacology and Physiology, 2011Microencapsulation of the BMDBM/HP-beta-CD complex in lipid microparticles significantly decreased the percutaneous penetration of the UV filter into the stratum corneum of human volunteers compared to the non-encapsulated sunscreen agent.
Journal of Pharmaceutical and Biomedical Analysis, 2011Following human skin application of an O/W emulsion containing 2% BMDBM loaded in lipospheres, 15% of the sunscreen accumulated in the uppermost layers of the stratum corneum without remarkably modifying skin permeation compared to unencapsulated sunscreen.
Skin Pharmacology and Physiology, 2008Dermal application of a sunscreen containing 10% homosalate in four volunteers resulted in delayed elimination with terminal half-times around 24 h and a bioavailability of cis-homosalate a factor of 2 lower than trans-homosalate, while metabolite ratios supported using oral-route urinary excretion fractions for dermal exposure assessments.
Archives of Toxicology, 2024Homosalate exhibited the highest permeation among tested filters with a relative permeability rate of 4.2% and a depth of 60 um, and specific thickeners and emulsifiers successfully reduced its permeation without inhibiting the skin permeation of niacinamide.
Photodermatology, Photoimmunology & Photomedicine, 2026An online-SPE-LC-MS/MS method successfully quantified specific urinary homosalate metabolites for up to 96 hours after dermal sunscreen application in a volunteer and detected metabolites exclusively in three German pilot participants who had used sunscreen within five days.
Analytica Chimica Acta, 2021Simulated real-life dermal sunscreen exposure in twenty human volunteers leads to the systemic bioavailability and urinary excretion of the UV filter 2-ethylhexyl salicylate and its metabolite, reaching concentration peaks at 7 to 8 hours with 70-80% of overall excretion within 24 hours.
Archives of Toxicology, 2019Controlled single dermal exposure to an EHS-containing sunscreen in three volunteers resulted in delayed systemic resorption with elimination half-lives between 6.6 and 9.7 hours, where the parent compound EHS occurred as the dominant urinary parameter.
Archives of Toxicology, 2024Dermal exposure to EHS-containing sunscreen leads to the urinary excretion of EHS as the main biomarker alongside major metabolites 5OH-EHS, 5cx-EPS, 4OH-EHS, and 5oxo-EHS, measured using an extended enzymatic hydrolysis and on-line SPE LC-MS/MS method.
Talanta, 2024Early application of sunscreen after ablative fractional skin resurfacing significantly increased the sensitization rate of the UV-filter, octocrylene, and the sunscreen compared to intact skin.
The Journal of Dermatological Treatment, 2015Dermal sunscreen exposure in 20 healthy volunteers led to plasma concentrations of avobenzone, octocrylene, and its metabolite CDAA reaching up to 11 μg/L, 25 μg/L, and 1352 μg/L, respectively.
Environment International, 2019UV filters octocrylene, octylmethoxycinnamate, and benzophenone-3 increase the generation of UV-induced reactive oxygen species in the nucleated epidermis above control levels when left on the skin surface for 60 minutes.
Free Radical Biology & Medicine, 2006Topical application of an antioxidant serum containing 15% ascorbic acid, 0.5% ferulic acid, and 1% tocopherol prevented particulate matter-induced degradation of extracellular matrix components, inflammation, and oxidative stress in the skin of 15 female volunteers compared to untreated controls.
Journal of Cosmetic Dermatology, 2025Dermatological products containing d-alpha tocopheryl acetate showed non-comedogenic potential with less than a 50% increase in microcomedones in 12 healthy male subjects compared to octyl palmitate.
Contemporary Clinical Trials Communications, 2021Topical application of an antioxidant mix containing 15% ascorbic acid, 0.5% ferulic acid, and 1% tocopherol prevented PM and UV-induced skin barrier perturbation, lipid peroxidation, inflammatory markers, MMP9 activation, and Type I collagen loss in 15 healthy females compared to untreated exposed skin.
Journal of Cosmetic Dermatology, 2024
Why other sunscreens fit oily acne-prone skin better
Biomimetic hyaluronic acid-stabilized zinc oxide nanoparticles selectively inhibited C. acnes, outperformed erythromycin in preclinical acne models, and safely reduced acne lesions and redness in a clinical trial.
Journal of Controlled Release, 2025Topical 0.5% hyaluronic-ZnO nanogel applied twice daily reduced inflammatory-lesion counts by 58% at week four in human subjects compared to baseline without causing erythema.
Biomedicines, 2025
Ingredients
Avobenzone, Homosalate, Octisalate, Octocrylene, Water, Aluminum Octenylsuccinate Starch, Glycerin, Polyester-27, Silica, Styrene Acrylates Copolymer, Phenoxyethanol, Isododecane, Arachidyl Alcohol, Beeswax, Ethylhexylglycerin, Neopentyl Glycol Diheptanoate, Acrylates C10-30 Alkyl Acrylate Crosspolymer, Behenyl Alcohol, Tocopherol Vitamin E, Arachidyl Glucoside, Glyceryl Stearate, Peg-100 Stearate, Potassium Hydroxide, Disodium Edta, Sodium Ascorbyl Phosphate
Behind this fit score
Lovi calculates every fit score from the full ingredient list with brand-independent rules our dermatologists and cosmetic chemists build and review, and personalizes every pick with AI trained on the real results of millions of users. Lovi trains its fit score models on a proprietary dataset built from more than 10,000 expert-labeled products and more than 100,000 simulated examples, following an internally consistent methodology presented at Cosmoprof, AMWC, and Skin of Color Update.
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Co-founder, Medical Director
Cosmetic chemist, cosmetologist, aesthetic products developer
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Co-founder, CEO and CTO
PhD in computer science, 3x US patent holder, ex-Google, ex-Yandex
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Dr. Sofía Perea Pérez, MD, MSc
Medical Board
Aesthetic medicine practitioner, MSc in Longevity and Anti-Aging Medicine
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Medical Board
Specialist dermatologist, MBBS, MD, IFAAD
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Medical Board
Cosmetic chemist, SCS, IFSCC member
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Medical Board, Medical Advisor
Dermatology MD
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Elina Nazarenko, MD
Medical Board
Dermatology and diagnostic consultant
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Victoria Derkova, MS
Medical Board
Cosmetic chemist, cosmetic development technologist
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