Abstract: An electrode structure includes: a plurality of pixel electrodes arranged separately from each other; and a plurality of dielectric layers laminated in a first direction with respect to the plurality of pixel electrodes, in which the plurality of dielectric layers includes: a first dielectric layer that spreads over the plurality of pixel electrodes in a direction intersecting with the first direction; and a second dielectric layer that includes dielectric material having a refractive index higher than that of the first dielectric layer, sandwiches the first dielectric layer together with the plurality of pixel electrodes, and has a slit at a position overlapping space between pixel electrodes adjacent when viewed from the first direction.

Abstract: It is intended to provide an aqueous suspension for nasal drops, which is easy to prepare, with maintaining superior long-term stability, good redispersibility and high retainability after the intranasal administration, as well as having good after feel. The aqueous suspension for nasal drops comprising containing the following (a), (b), (c), (d), (e) and (f): (a) A compound represented by the following formula (1) wherein R is hydroxyl or cyclohexylcarbonyloxy, or solvate thereof; (b) crystalline cellulose-carmellose sodium 0.1-5% by weight; (c) hydroxypropylcellulose 0.05-1% by weight; (d) nonionic surfactant 0.001-0.2% by weight; (e) moistening agent; and (f) buffering agent.

Abstract: A transdermal absorption promotion composition comprising the following components (a), (b), and (c) and a transdermal absorption preparation comprising the following components (a), (b), (c), and (d) are disclosed. (a) propylene glycol (b) a polyol fatty acid ester (c) lauromacrogol (d) a drug component The transdermal absorption promotion composition and transdermal absorption preparation not only exhibit an excellent transdermal absorption promotion effect, but also exhibit superior skin-permeability, even if a drug having a relatively high lipophilic property and poor transdermal absorbability is used, exhibit a favorable feeling of use, and are safe and stable.

Abstract: An antifungal and/or antimycotic external preparation for nail, which comprises neticonazole or a salt thereof and a basic substance.

Abstract: The present invention relates to a sustained-release suppository preparation characterized by comprising an acidic drug or a salt thereof which can be absorbed by rectal administration and an acidic compound or a pH buffering agent. The sustained-release suppository preparation of the present invention exhibits no rapid increase in blood concentration immediately after the administration and maintains its action for a long period of time. Thus, it is safer and exhibits a better therapeutic effect.

Abstract: Ointments are disclosed, which contain (a) 0.05-1 wt. % of deprodone propionate and (b) 89-99.95 wt. % of a base formed of white petroleum and a liquid hydrocarbon. The ointments may additional contain (c) 1-10 wt. % of a polyhydric alcohol.

Abstract: Antimycotic external imidazole preparations are disclosed. They contain the following ingredients:(a) 0.1-5 wt. % of (E)-1-[2-methylthio-1-[2-(pentyloxy)phenyl]ethenyl]-1H-imidazole hydrochloride;(b) 0.01-3 wt. % of a basic substance; and(c) an external preparation base.

Abstract: Water-containing external preparations are disclosed, which contain, as essential ingredients, (a) 0.05-1 wt. % of deprodone propionate and (b) 1-20 wt. % of a polyhdric alcohol.