The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 18, 2016

Filed:

Mar. 31, 2014
Applicant:

Johnson & Johnson Consumer Inc., Skillman, NJ (US);

Inventors:

Ying Sun, Belle Mead, NJ (US);

Jeffrey M. Wu, Princeton, NJ (US);

Ali Fassih, Franklin Park, NJ (US);

Assignee:

Johnson & Johnson Consumer Inc., Skillman, NJ (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K 9/14 (2006.01); A61K 9/50 (2006.01); A61K 47/10 (2006.01); A61K 31/192 (2006.01); A61K 9/00 (2006.01); A61K 47/12 (2006.01); A61K 8/49 (2006.01); A61K 8/02 (2006.01); A61Q 7/00 (2006.01); A61K 47/02 (2006.01); A61K 47/22 (2006.01); A61K 47/18 (2006.01); A61K 8/25 (2006.01); A61K 8/34 (2006.01); A61K 8/36 (2006.01); A61K 8/11 (2006.01); A61K 31/196 (2006.01); A61K 31/40 (2006.01); A61K 31/405 (2006.01); A61K 31/60 (2006.01); A61K 31/616 (2006.01);
U.S. Cl.
CPC ...
A61K 9/501 (2013.01); A61K 8/022 (2013.01); A61K 8/11 (2013.01); A61K 8/25 (2013.01); A61K 8/345 (2013.01); A61K 8/36 (2013.01); A61K 8/4953 (2013.01); A61K 9/0014 (2013.01); A61K 31/192 (2013.01); A61K 31/196 (2013.01); A61K 31/40 (2013.01); A61K 31/405 (2013.01); A61K 31/60 (2013.01); A61K 31/616 (2013.01); A61K 47/02 (2013.01); A61K 47/10 (2013.01); A61K 47/12 (2013.01); A61K 47/18 (2013.01); A61K 47/22 (2013.01); A61Q 7/00 (2013.01); A61K 2800/41 (2013.01); A61K 2800/652 (2013.01);
Abstract

A powder is disclosed including core/shell particles having an average particle size of less than 1000 microns, each particle contains a liquid core that is substantially free of water and includes A) a polar liquid having a percent surface polarity of at least 24%, an active ingredient, and C) from about 0.1% to about 20% by weight of at least one solubility enhancing agent that is not an active ingredient; and a shell comprising hydrophobic particles. The powder can be used to topically administer the active ingredient to a human or animal.


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