In the context of the revision of the guideline on ‘Excipients in the label and package leaflet of medicinal products for human use’ (CPMP/463/00 Rev. 1)
Draft report published in support to the Q&A document.
For information only
Background review for sodium laurilsulfate used as an excipient
23 July 2015
EMA/CHMP/351898/2014
Committee for Human Medicinal Products (CHMP)
EMA/CHMP/351898/2014
Committee for Human Medicinal Products (CHMP)