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Comment
. 2020 Jun;182(6):1345-1347.
doi: 10.1111/bjd.18803. Epub 2020 Feb 3.

Effect of sunscreen application under maximal-use conditions on plasma concentration of sunscreen active ingredients: a critical appraisal

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Comment

Effect of sunscreen application under maximal-use conditions on plasma concentration of sunscreen active ingredients: a critical appraisal

M Charalambides et al. Br J Dermatol. 2020 Jun.
No abstract available

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References

    1. Matta MK, Zusterzeel R, Pilli NR et al. Effect of sunscreen application under maximal use conditions on plasma concentration of sunscreen active ingredients: a randomized clinical trial. JAMA 2019; 321:2082-91.
    1. US Food and Drug Administration (FDA). Sunscreen drug products for over-the-counter human use: proposed rule. Fed Regist 2019; 84:6204-75.
    1. European Commission. Scientific Committee on Consumer Safety. Opinion on 4-methylbenzylidene camphor. SCCP/1042/06. Available at: https://ec.europa.eu/health/ph_risk/committees/04_sccp/docs/sccp_o_075.pdf (last accessed 11 December 2019).
    1. European Commission. Scientific Committee on Consumer Safety. Opinion on 2-(4-(2-(4-diethylamino-2-hydroxy-benzoyl)-benzoyl)-piperazine-1-carbonyl)-phenyl)-(4-diethylamino-2-hydroxyphenyl)-methanone, HAA299, as UV filter in sunscreen products. SCCS/1533/14. Available at: https://ec.europa.eu/health/scientific_committees/consumer_safety/docs/s... (last accessed 11 December 2019).
    1. Schulz KF, Altman DG, Moher D. CONSORT 2010 statement: updated guidelines for reporting parallel group randomized trials. Ann Intern Med 2010; 152:726-32.

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