La Roche-Posay Anthelios Clear Skin Dry Touch Sunscreen SPF 60 for oily acne-prone skin
Cell-Ox Shield Technology
Avobenzone
Homosalate
Octisalate
OctocryleneSuperior
- SuperiorOily Skin Fit
- SuperiorEffectiveness
- ExcellentSafety
One of the best sunscreens for oily acne-prone skin.
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
- Excellent suitability for your oily skin is provided by silica and perlite, which mattify and absorb excess sebum, while Cassia Alata Leaf Extract and tocopherol offer antioxidant benefits and soothe your skin, addressing your concerns with acne, blemishes, and breakouts.
- The formulation offers superior sun protection with high concentrations of avobenzone, homosalate, octisalate, and octocrylene, shielding your skin from UV radiation.
- The safety profile is excellent, with no risks of irritation for your oily skin due to the absence of harsh ingredients and the presence of soothing components.
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.
People Say
★4.3Overall rating based on 2.5k+ reviewsBased on a very large amount of data, this sunscreen is highly recommended for oily and acne-prone skin, offering effective sun protection with a matte finish that controls shine. While many users praise its non-comedogenic properties, a significant number report issues with the product pilling or flaking during application, which should be taken into account.
Highlights
Severe pilling Mostly Mentioned
- “balls up”
- “flakes off”
- “pills like crazy”
Acne-safe formula Often Mentioned
- “only sunscreen”
- “won't cause breakouts”
- “clog pores”
- “cystic acne”
Excellent oil control Often Mentioned
- “shine-free”
- “matte”
- “heat and humidity”
Fragrance-free/gentle Sometimes Noted
- “sensitive skin”
- “unscented”
- “no irritation”
- “no stinging”
High sun protection Sometimes Noted
- “SPF 60”
- “prevents sunburn”
- “sun spots”
Difficult texture Sometimes Noted
- “thick”
- “paste-like”
- “hard to spread”
Visible white cast Sometimes Noted
- “purple residue”
- “ghostly white residue”
- “takes time to fade”
Drying effect Rarely Noted
- “too drying”
- “leaving dry patches”
- “makeup look cakey”
Sources: lovi.care, walmart.com, dermstore.com, target.com, ulta.com, lovelyskin.com, and more
Questions and answers
What makes La Roche-Posay Anthelios Clear Skin Sunscreen one of the best fits for oily acne-prone skin?
This sunscreen is one of the best fits because silica and perlite soak up excess oil to keep your skin matte, while antioxidants like tocopherol help calm breakouts and blemishes. It also has a very safe formula that is unlikely to cause irritation on oily skin.
Which ingredients make this sunscreen a good fit for oily acne-prone skin?
Silica and perlite make this sunscreen a great fit for your oily skin by absorbing excess shine, while tocopherol helps soothe breakouts. Chemical filters like avobenzone, homosalate, octisalate, and octocrylene are unlikely to cause irritation.
What does Cell-Ox Shield do for oily acne-prone skin?
Cell-Ox Shield helps protect oily acne-prone skin from sun damage that can worsen breakouts and cause dark marks. Sunscreens specifically formulated for this skin type improve symptoms and enhance your overall acne routine.
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.
Where does this sunscreen 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 very safe and unlikely to cause irritation on oily skin while keeping shine under control.
Can I use this sunscreen with retinol, and in what order?
You can use this sunscreen in the morning as the final step before makeup, always after applying your moisturizer. It is unlikely to cause irritation or interfere with your retinol routine because it has a gentle formula designed for acne-prone skin.
How often should I use this sunscreen?
Use this sunscreen every morning as the final step of your daytime routine. It is very safe and unlikely to irritate your skin when used daily.
Can this sunscreen clog pores, cause breakouts or purging for oily acne-prone skin?
This sunscreen is unlikely to clog pores or cause breakouts on oily skin, as it contains ingredients that absorb excess oil and is very gentle. Chemical sunscreens like this one generally show little to no risk of irritation or related issues on human skin.
Is this sunscreen fragrance-free and alcohol-free?
Yes, it has no fragrance and no drying alcohol. Behenyl alcohol, arachidyl alcohol, and stearyl alcohol are fatty alcohols, which soften the skin.
What the research says
A topical serum containing vitamin C, vitamin E, and raspberry leaf cell culture extract improved skin color, elasticity, radiance, smoothness, scaliness, and wrinkles compared to the untreated contralateral side in fifty female volunteers.
Journal of Cosmetic Dermatology, 2020Incorporating rosmarinic acid into sunscreens enhanced the in vivo SPF of octocrylene by over 157% and reduced lipid peroxidation in the human stratum corneum.
Antioxidants, 2025Chemical 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, 2025Topical application of an aqueous gel containing 0.1% w/w naringenin demonstrated in vitro safety, significantly reduced UV-induced stratum corneum lipid peroxidation, and showed in vivo anti-inflammatory efficacy against methyl nicotinate-induced inflammation in human participants compared to a blank gel and untreated area, while chlorogenic acid, apigenin, and kaempferol displayed pro-oxidant profiles.
Frontiers in Chemistry, 2024Sunscreens containing Mexoryl SX provide superior protection against UVA- and solar-simulated radiation-induced biological damage, including pigmentation, DNA damage, immune suppression, and dermal alterations, compared to formulations without it in human volunteers and patients.
Photodermatology, Photoimmunology & Photomedicine, 2008Mexoryl SX (5%) efficiently prevents UVA-induced skin alterations including pigmentation, stratum corneum thickening, and protein expression changes in human skin.
Journal of Photochemistry and Photobiology. B, Biology, 1998Topical application of both a UVB absorber and a broad-spectrum Mexoryl SX sunscreen effectively prevented UVB-induced damage in in vitro reconstructed human skin, whereas only the Mexoryl SX-containing preparation successfully prevented UVA-specific dermal fibroblast disappearance.
Photochemistry and Photobiology, 2000Encapsulation 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, 2019The 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, 2024Controlled 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, 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, 2006
Ingredients
Avobenzone, Homosalate, Octisalate, Octocrylene, Water, Silica, Dicaprylyl Carbonate, Styrene Acrylates Copolymer, Butyloctyl Salicylate, Methyl Methacrylate Crosspolymer, Nylon-12, Peg-100 Stearate, Glyceryl Stearate, Perlite, Beeswax, Ammonium Polyacryloyldimethyl Taurate, Phenoxyethanol, Peg-8 Laurate, Behenyl Alcohol, Sodium Stearoyl Glutamate, Chlorphenesin, P-Anisic Acid, Xanthan Gum, Tocopherol, Disodium Edta, Arachidyl Alcohol, Diethylhexyl Syringylidenemalonate, Propylene Glycol, Cassia Alata Leaf Extract, Maltodextrin, Stearyl Alcohol, T-Butyl Alcohol, Caprylic Capric Triglyceride
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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