CPC A61K 8/99 (2013.01) [A61K 8/022 (2013.01); A61K 8/042 (2013.01); A61K 8/19 (2013.01); A61K 8/34 (2013.01); A61K 8/37 (2013.01); A61K 8/671 (2013.01); A61K 8/735 (2013.01); A61K 8/88 (2013.01); A61K 8/922 (2013.01); A61K 8/9789 (2017.08); A61K 9/06 (2013.01); A61K 9/19 (2013.01); A61K 31/07 (2013.01); A61K 35/741 (2013.01); A61K 47/14 (2013.01); A61K 47/34 (2013.01); A61K 47/44 (2013.01); A61K 47/46 (2013.01); A61Q 19/00 (2013.01); A61K 2800/524 (2013.01); A61K 2800/594 (2013.01)] | 2 Claims |
1. A dermatological composition consisting of:
an anhydrous formulation of:
about 0.1% to about 5% by mass of a dry growth-arrested genetically modified strain of Cutibacterium acnes (C. acnes) that remains in a dormant state for at least six months and up to about 2 years;
about 55% to about 95% by mass of one or more anhydrous emollients comprising ethyl olivate or Olea europaea leaf extract; and
about 1% to about 15% by mass of one or more anhydrous gelling agents comprising Polyamide-3.
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