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Background/purpose: Visible light (VL), a substantial component of solar radiation, contributes to skin photodamage, including hyperpigmentation and erythema. Tinted sunscreens have emerged as effective tools for mitigating VL-induced effects, yet challenges remain in their adoption and utilization. This review updates recent evidence on their clinical efficacy and explores obstacles constraining their broader recognition and utilization.
Methods: A comprehensive search was performed on December 28, 2024, across MEDLINE, PubMed, the Cochrane Database of Systematic Reviews, and Web of Science using Mesh Terms "visible light," "sunscreens," and keywords related to "tinted sunscreen." A total of 89 articles were initially retrieved. After screening for relevance and recent publication, 67 articles were selected for detailed review.
Results/conclusion: Tinted sunscreens outperform non-tinted products in protecting against VL-induced photodamage and managing melasma relapse, extending photoprotection beyond UV radiation. However, their adoption is limited by the lack of standardized guidelines and unified evaluation metrics, and inadequate shade diversity for skin of color. Future research should focus on expanding shade ranges, establishing comprehensive evaluation standards, and refining formulations with active ingredients.
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http://dx.doi.org/10.1111/phpp.70033 | DOI Listing |
Exp Dermatol
September 2025
L'Oréal Research and Innovation, Aulnay sous Bois, France.
As hyperpigmentation can worsen with exposure to ultraviolet (UV) and visible light (VL), sunscreens with well-balanced UVB/UVA protection and VL-blocking pigments are recommended. Assessing efficiency against VL-induced pigmentation is then mandatory. Recently, an in vivo pigmentation assessment allowing a VL protection factor (pVL-PF) determination, and an in vitro predictive method based on transmittance measures were introduced.
View Article and Find Full Text PDFJ Am Acad Dermatol
August 2025
Department of Dermatology, University of Washington, Seattle, WA. Electronic address:
Int J Dermatol
August 2025
Division of Dermatology, Department of Medicine, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Sun protection is critical for the prevention and management of skin cancer and other photosensitive dermatoses in South Africa's diverse population. This review expands on previously published sun protection advice for skin cancer prevention by providing tailored advice for individuals with specific dermatological conditions. Recent advances in sunscreen technology, including enhanced protection for long-wave UVA1, visible light, and infrared radiation; inorganic sunscreens with more cosmetic acceptability; and the addition of other active ingredients unrelated to sun protection, are discussed in the context of specific dermatoses.
View Article and Find Full Text PDFDermatol Ther (Heidelb)
September 2025
Department of Dermatology, Weill Cornell Medical College, New York, NY, USA.
Introduction: Topical treatment with hydroquinone 4% and hydroquinone-based preparations is the gold standard of care for melasma; however, it is limited by complications. 2-Mercaptonicotinoyl glycine (Melasyl™) is a new active ingredient targeting melanin synthesis without impairing the tyrosinase enzyme, with proven efficacy and safety. This study assessed the non-inferiority of a new facial depigmenting serum Mela B3 (MB3), containing 0.
View Article and Find Full Text PDFPhotodermatol Photoimmunol Photomed
July 2025
Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Background/purpose: Visible light (VL), a substantial component of solar radiation, contributes to skin photodamage, including hyperpigmentation and erythema. Tinted sunscreens have emerged as effective tools for mitigating VL-induced effects, yet challenges remain in their adoption and utilization. This review updates recent evidence on their clinical efficacy and explores obstacles constraining their broader recognition and utilization.
View Article and Find Full Text PDF