Abstract: The present disclosure is directed to table mount for mounting a touchscreen device to a surgical table. The table mount includes a clamp configured to releasably secure the table mount to the table, a first arm rotatably connected to the clamp and configured to extend vertically from the surgical table, a second arm rotatably connected to the first arm, and a touchscreen device docking assembly rotatably connected to the second arm and configured to hold a touchscreen device.

Abstract: A health promoting apparatus to benefit health of a user based on medical factors underlying moderate exercise, comprises: an oscillation generator configured to oscillate a head of the user in a vertical direction or an anteroposterior direction; and an oscillation controller connected to the oscillation generator, and configured to control the oscillation generated by the oscillation generator. The oscillation controller is configured to control the oscillation generator to apply a shear stress to cells in a brain of the user by moving interstitial fluid in the brain, in order to promote the health of the user.

Abstract: A fluidic actuator unit that includes a joint, a first arm coupled to the joint, a second arm coupled to the joint; and an inflatable bellows actuator extending between a first and second plate associated with the joint, the inflatable bellows actuator defining a bellows cavity, the inflatable bellows actuator configured to extend along a length of the bellows actuator when inflated by introducing fluid into the bellows cavity.

Abstract: The disclosure includes an exoskeleton network. The exoskeleton network includes an exoskeleton system that has one or more sensors and a memory; a user device that is local to the exoskeleton system and that operably communicates with the exoskeleton system; and a classification server that operably communicates with at least one of the exoskeleton system and the user device. The exoskeleton network performs feature extraction on sensor data obtained from the one or more sensors to generate feature-extracted sensor data and performs label derivation on the feature-extracted sensor data to generate labeled sensor data.

Abstract: A harness used for a locomotor training of a patient, such as a pediatric patient, is provided. The harness has a bottom strap, such as two leg straps, for providing pelvic support to the patient and a pelvic band for providing waist support to the patient. The bottom strap is releasably connected to the pelvic band. Multiple lifting straps are connected to the pelvic band. The lifting straps can be manipulated to provide partial weight support to the patient. The harness has circumferential bands of varying widths that can be easily added and removed to provide maximum trunk support to minimal or no trunk support across the length of the trunk. This allows the harness to dynamically meet the needs of trunk support as the patient advances.

Abstract: The group of useful models has to do with physiotherapeutic devices, in particular massage brooms, the task of which is to enhance their effectiveness. The massage broom has metal bristles, which have been put together compactly in a portion of the massage broom in order to form a handle, and in the remaining portion of the massage broom the bristles are separated from one another. In one of the variants, the handle or its part is formed by the metal sleeve and by the additional metal sleeve. The bristles are passed through these sleeves. Thus, the possibility exists that sound waves can be generated upon tapping. Various instances of embodiments of massage brooms in four variants are also described.

Abstract: The present disclosure is drawn to skin care devices. An example skin care device can include skin-rejuvenation head with a first external region including an array of skin-cleansing bristles and a second external region including an auxiliary skin-treatment appliance of a different type than the skin-cleansing bristles. The skin-rejuvenation head can include a vibrational motor positioned therein to provide vibratory oscillation to both the skin-cleansing bristles and the auxiliary skin-treatment appliance. A support rod can be mechanically coupled to the skin-rejuvenation head. A handle can include a neck portion and a grip portion, with the support rod also coupled to the handle. The neck portion can be proximal to the skin-rejuvenation head and the grip portion can be distal to the skin-rejuvenation head. The neck portion can include an energy dampening sleeve around the support rod, leaving a gap around the support rod.

Abstract: A device (900) includes a leg engaging section (101) and a foot engaging section (102 intersecting at a heel receiver (103). The leg engaging section and the foot engaging section defining a leg insertion aperture (104). A first compression wrap member (301) and a second compression wrap member (302) extend from the leg engaging section. An inflatable bladder (501) can be disposed along the leg engaging section between the leg insertion aperture and a compressible cushion layer (902). The inflatable bladder can be selectively inflatable through a connection tube (502) exiting the inflatable bladder at a non-orthogonal angle (504) relative to an edge (507) of the inflatable bladder. The leg engaging section can define at least one channel (1002) to permit the connection tube to exit the device.

Abstract: A light therapy system is made up of a pressure cuff system having a cuff that is positionable on or near a body part of a user and that can receive pressurized air to selectively pressurize and depressurize the cuff and a light emitting system having a supporting structure and a light emitter positioned on the supporting structure, the light emitter being controllably powerable. The supporting structure is positionable on an interior surface of the cuff so that the light emitter can direct light onto the body part. The light therapy system can further include a controller capable of controllably powering the light emitter, wherein controller can adjust the intensity or duration of the light directed onto the body part in response to an input or measurement related to a condition of the body part. A photometer can be provided separately or integrally to measure the condition of the body part. A method of providing light therapy is also provided.

Abstract: A kit is disclosed for facilitating the supply and return of a system for stimulating venous and arterial circulation in a patient to prevent deep vein thrombosis, which includes a left and right set of inflatable garment sleeves that are disposable, a pair a rechargeable battery powered pump assemblies for inflating the sleeves and that are reusable, a power supply adapter for recharging the pump assemblies and that is reusable, and a shipping carton for returning the pump assemblies and adapter to a supplier after the patient is ambulatory and the risks of deep vein thrombosis have ended.

Abstract: A heated massaging joint brace comprising a brace structure and a first material. A plurality of massaging elements are disposed on an interior of the first material. A heating element is further disposed on the interior of the first material. A power source is operably coupled to the heating element and the plurality of massaging elements. A controller is disposed on an exterior of the brace structure. The controller can control the speed of the massaging elements and the heat of the heating element. The heated massaging brace can be attached to a wearer to heat and massage the area covered by the brace.

Abstract: A system and method for automated generation of control signals for sexual stimulation devices from videos of sexual activity. The system and method use annotation data indicating comprising indications of movements in the video corresponding to sexual activity to generate control signals for compatible sexual stimulation devices. The annotation data may be generated manually or automatically. Device control signals may be generated directly from the annotation data and synchronized with a video, or may be processed through a series of machine learning algorithms to generate models of “typical” sexual activity represented in the videos, which models are then used to generate signals for the sexual stimulation device.

Abstract: A finger-splinting sheath device is provided for use as a self-treatment aid in assisting a bowel in a patient suffering from complications of pelvic organ prolapse, namely rectocele. The finger-splinting sheath device generally includes a monolithic molded body including a flange-element, and a sheath-element having a proximal end and a distal end, wherein the sheath-element is coupled to the flange-element at the proximal end and is closed at the distal end. The sheath-element generally includes an elliptical cross-section configured to receive two-fingers therein, wherein the sheath-element functions to splint the two fingers during use. A method for using the device includes inserting the device with two fingers within the sheath-element into the vagina and applying pressure to the vaginal walls to assist a bowel movement.

Abstract: A percussive massage device includes an enclosure having a cylindrical bore that extends along a longitudinal axis. A motor has a rotatable shaft that rotates about a central axis perpendicular to the longitudinal axis. A crank coupled to the shaft includes a pivot, which is offset from the central axis of the shaft. A transfer bracket has a first end portion coupled to the pivot of the crank. A flexible transfer linkage has a first end coupled to a second end portion of the transfer bracket. A piston has a first end coupled to a second end of the transfer linkage. The piston is constrained to move within a cylinder along the longitudinal axis of the cylindrical bore. An applicator head has a first end coupled to a second end of the piston and has a second end exposed outside the cylindrical bore for application to a person receiving treatment.

Abstract: A flexible vibrating module with flexible radiating arms outwardly projecting around the module, with each arm having an associated coin motor which can optionally be operated at high frequency or low frequency or pulsing frequency, is shown in combination with a wrap having a snap in flexible grommet for the module to consistently orient properly the module with respect to a patient's muscles or joints.

Abstract: Systems, apparatuses, and methods directed to the collection and analysis of data related to a patient during an emergency advanced airway management process. The collected data may be obtained using various types of sensors, with the data collection process being managed or coordinated by a suitable system, such as a combination monitor-defibrillator. The monitor-defibrillator (alone or in combination with other system elements, such as a wired or wireless communications capability, a processor, data storage, etc.) may include a capability to process some or all of the acquired data, and in response indicate to a user when some of the collected data may be unreliable.

Abstract: The present invention is applicable to the field of cosmetic instruments. The present invention discloses a nozzle rotating mechanism and a facial steaming apparatus, wherein the nozzle rotating mechanism comprises a nozzle and a driving mechanism for rotating the nozzle, the nozzle being located outside an axis of a nozzle shaft, the axis of the nozzle being parallel to or forming an angle with the nozzle shaft. The nozzle rotating mechanism is driven to rotate by a driving mechanism when it is in use. Since the axis of the nozzle is parallel to or forming an angle with the nozzle shaft, i.e., the axis of the nozzle and the nozzle shaft are not on the same line, so the nozzle must form a larger radius of rotation relative to the axis of the nozzle shaft when the nozzle rotates on the nozzle shaft. Therefore, the nozzle can form a larger area, which can increase the area of steam injection, better suit requirements from different users, and improve the user experience.

Abstract: The invention concerns a portable device for transmitting electromagnetic waves. It is capable, when arranged at a surface, of transmitting waves having a power flux density of at least 0.5 milliwatts per square centimeter of surface area and a frequency value of between 3 and 120 gigahertz. The device is, moreover, capable of simultaneously exposing at least 2.5 square centimeters of the surface to the waves.

Abstract: A drug delivery system includes a delivery container, a first drug insertion port, at least one additional drug insertion port, and an IV connection port. The delivery container includes upper, lower, first side, and second side portions, and further includes a tapered region extending between the first side portion and the second side portion. The first drug insertion port is positioned at the lower portion of the delivery container and has a first coupling mechanism. The at least one additional drug insertion port is also positioned at the lower portion of the delivery container, but includes a second coupling mechanism that is different than the first coupling mechanism. The IV connection port is positioned at the lower portion of the delivery container adjacent to a lower portion of the tapered region.

Abstract: This packaging device (1) is configured to support medical containers (100), said packaging device (1) comprising a first nest (4a) including a first set of supporting units (42a) configured to support a proximal end (105) of a first plurality of medical containers (100a) and a second nest (4b) including a second set of supporting units (42b) configured to support a proximal end (105) of a second plurality of medical containers (100b), the first set of supporting units (42a) and the second set of supporting units (42b) being configured to maintain said first plurality of medical containers (100a) and said second plurality of medical containers (100b) in an inverted position relative to each other. The first nest (4a) further comprises guiding means configured to maintain a distal end (106) of the second plurality of medical containers (100b) while the second nest (4b) comprises guiding means configured to maintain a distal end (106) of the first plurality of medical containers (100a).

Abstract: A warming device and system for warming medical gel to a comfortable temperature prior to application to a patient. A warming chamber configured to receive one or more gel containers (e.g., packets or bottles) disposed in a horizontal orientation with a cover sealing the chamber. Multiple protrusions and/or depressions disposed on an inside surface of the chamber can be used to soften thermal conduction of heat to the gel containers and inhibit hot spots. A flexible heating element and an intermediate thermal conducting member can extend up one or more sides of the warming chamber. Multiple buttons can be used to set different gel temperature settings.

Abstract: This invention discloses a single-needle medication mixer, dual hard ports, and a soft intravenous bag, pertaining to the field of medical apparatus technologies. The medication mixer comprises a base, a medication mixing passage, a medication mixing cup, and a piercing needle. The base, the medication mixing passage and the medication mixing cup are integrally formed, the medication mixing cup consists of cup wall and cup bottom, the lower end of the medication mixing passage penetrates through the base, and the upper end penetrates through the cup bottom; the upper end of the medication mixing passage is provided with the piercing needle having a hollow passage, the lower end of the piercing needle is connected to the upper end of the medication mixing passage in a sealing way, and the hollow passage is communicated therewith. The medication mixer of this invention is convenient to use and has no potential safety hazard.

Abstract: This invention discloses a medication mixer, dual hard dual ports, and a soft intravenous bag. The medication mixer comprises a base, a medication mixing passage, a medication mixing cup, and a cross needle which are integrally formed. The medication mixing cup consists of a cup wall and a cup bottom. The cross needle consists of an integrated needle plate, and an upper needle and lower needle with hollow passages which are communicated with each other. The lower end of the medication mixing passage penetrates through the base, with the upper ends penetrating through the cup bottom. A membrane is arranged in the medication mixing passage between the base and the cup bottom, and a rubber plug is arranged in the medication mixing passage between the membrane and the cup bottom. A limit protrusion is arranged on an inner wall of the cup wall.

Abstract: A point of care device for securely dispensing medication includes an enclosure sized to contain medication containers, a holding element accessible from outside the enclosure to receive medication containers from the enclosure, a dispenser to dispense medication from the enclosure to the holding element, and a securable panel configured to provide access to the enclosure for retrieval or replenishment of the medication containers within the enclosure, and a computing device operable to control the dispenser to dispense medication to the holding element based on various conditions. Specifically, the point of care device can be configured to dispense medication based on detecting that an authorized user is accessing the device, based on a timer in conjunction with known medication regimen, or based on patient or physician demand, or based on biometric information concerning the user.

Abstract: A tamper-resistant pill and/or capsule dispenser for attachment to an electronic control and communication unit including inter alia, an electric actuator mechanism, a microprocessor, a graphical user interface and a communications unit, the dispenser including sensors operative under control of said electronic control and communication unit to monitor and dispense prescribed dosages of medications or vitamin supplements in pill and/or capsule form and help control, track and maintain a record of pills and/or capsules dispensed to a patient to ensure that the dispensed product is not improperly removed from or replaced in the dispenser, said dispenser comprising: a generally cylindrical housing having an open top, and a generally closed bottom, except for a pill dispensing opening formed in a lower side portion of the cylindrical housing; a cylindrical sleeve open at its top end and closed at its bottom end, said sleeve being eccentrically disposed within said cylindrical housing and away from the side of sai

Abstract: A compressible device for use on a drinking container includes a base and at least one spill-proof unit. The base includes a base wall defining a liquid flow passage, and a separation wall connected to the base wall and dividing the liquid flow passage into a liquid inlet zone and a liquid outlet zone. The at least one spill-proof unit includes a through slot formed in the separation wall and communicating with the liquid outlet zone, and a spill-proof seat including a plate body opposite to the through slot and formed with a first slit. When the plate body is compressed and deformed, the first slit is opened to communicate the liquid inlet zone with the liquid outlet zone through the through slot.

Abstract: Systems and devices for providing readily accessible and unassisted oral hydration to a patient or other individual. A hydration system of the present disclosure may include a container for holding a quantity of liquid, a hydration tube extending from the container, and a hydration control valve through which a user may access the liquid by pushing or pressing on a lever. The hydration control valve may be, or be similar to, a pinch valve or bite valve arranged across a tube, such that by opening the valve, water may be permitted to flow through the tube. The valve may be arranged within a valve casing having a hydration tube coupling portion and a mouthpiece.

Abstract: An automatic breastfeeding method of a premature infant is disclosed, which includes a preparation stage, an active lactation stage, a passive lactation stage and a rest stage. The invention also provides an automatic breastfeeding machine used for the automatic breastfeeding method of a premature infant, comprising a stomach tube, a lactation supply device, a detector and a control device. According to the invention, a self-sucking ability of the premature infant is trained, normal circulation of a mouth-pharyngeal-gastric-intestinal reflex of the premature infant is realized, and nutritional requirements of the premature infant are ensured in the case of taking differences of the premature infants into account, so that the premature infants have no difference with term infants in care, diet, neurological development and growth and development in the future.

Abstract: An oral varnish comprising a combination of two different viscosity dimethicone components, wherein the difference between the two different viscosity dimethicone components is about 2.0 million cP or greater; and comprising at least one active ingredient, which is preferably a fluoride donor.

Abstract: Radically polymerizable dental material, which contains a combination of a thiourea derivative, a hydroperoxide and at least one peroxide as well as a transition metal compound as initiator system for the radical polymerization.

Abstract: A dental curable composition which comprises a radically polymerizable monomer component (A), a polymerizing catalyst (B) and an inorganic granular material (C), characterized in that: the radically polymerizable monomer component (A) contains a bifunctional monomer (A-1) represented by the following formula (?), RP—SP1—RP ??(?) where, RP is a radically polymerizable group represented by CH2?C(R)—COO— or CH2?C(R)—CONH—, wherein R is a hydrogen atom or a hydrocarbon group having 1 to 3 carbon atoms, and SP1 is a hydrocarbon group having 5 to 15 carbon atoms, and the content of the bifunctional monomer (A-1) in the radically polymerizable monomer component (A) is 5 to 40% by mass under a condition that the content of a diluting monomer (A-2) represented by the following formula (?), RP—SP2—RP ??(?) where, RP is as defined in the above formula (?), and SP2 is an aliphatic hydrocarbon group different from.

Abstract: A polymerisable dental composite material comprising (i) 60 to 85% by weight of an inorganic filler component comprising at least one tectosilicate and optionally at least one dental glass and/or at least one amorphous metal oxide, (ii) 10 to 40% by weight of a mixture of at least two different urethane(meth)acrylates, (iii) 0.01 to 5% by weight of at least one di-, tri-, tetra- or multi-functional monomer not being a urethane(meth)acrylate, (iv) 0.01 to 10% by weight of at least one initiator, an initiator system and optionally at least one stabiliser and optionally at least one pigment, wherein the total composition of the composite material amounts to 100% by weight, and a polymerised composite material having a flexural strength of greater than or equal to 240 MPa and an elastic modulus of 16 to 20 GPa for the production of indirect dentures.

Abstract: Radically polymerizable dental material, which contains a combination of a thiourea derivative and a hydroperoxide according to the following Formula (I) as initiator system for the radical polymerization:

Abstract: Radically polymerizable dental material, which contains a combination of a thiourea derivative, a hydroperoxide and at least one peroxide as initiator system for the radical polymerization.

Abstract: In some embodiments, a cosmetic composition includes a powder formulation, at least one additive, and at least 20% water by weight. The powder formulation includes silica silylate, methyl methacrylate crosspolymer, microcrystalline cellulose particles, and boron nitride. In some embodiments, the powder formulation includes silica silylate in an amount of about 0.05% to about 1.0%, methyl methacrylate crosspolymer in an amount of about 0.1% to about 5.0%, microcrystalline cellulose particles in an amount of about 0.1% to about 3.0%, a first portion of boron nitride in an amount of about 0.1% to about 3.0%, and a second portion of boron nitride in an amount of about 0.1% to about 5.0%, all by weight of the cosmetic composition. A method of providing a skin smoothing and radiant optical effect to skin includes applying a cosmetic composition including water, at least one additive, and a powder formulation to the skin.

Abstract: Disclosed are a cosmetic composition having increased skin contact and makeup persistence and a method of manufacturing the same. The method includes: forming a powder continuous phase by rapidly mixing a powder and a film-forming agent; and obtaining a cosmetic composition in which a surface of the powder is compounded with the film-forming agent by heating the powder continuous phase for a predetermined time. In an embodiment, the cosmetic composition is manufactured by the method. In an embodiment, the cosmetic composition includes 5 wt % to 30 wt % of a powder, 0.1 wt % to 10 wt % of a film-forming agent, 10 wt % to 30 wt % of a silicone oil, and 0.1 wt % to 10 wt % of a spherical powder.

Abstract: A composition for a hydrogel sheet may include a cellulose ether, a gelling agent, and a gelling promoter, where an aqueous 2 wt % solution of the cellulose either may have a viscosity of 3 cps to 300 cps, as measured under a condition of 20 ° C. using an Ubbelohde viscometer. The gelling agent may include one or more selected from the group consisting of carrageenan, locust bean gum, mannose, and water chestnut flour.

Abstract: Disclosed is a personal care composition comprising: a) a porous particle; b) a film forming polymer; and c) a cosmetically acceptable carrier which is a water and oil emulsion; wherein the porous particle has oil absorption value in the range of 50g/100g to 1500g/100g; wherein the porous particle is selected from porous silica, cellulose, acrylic polymer, nylon and ethylene/methacylate copolymer hollow sphere coated with porous silica; wherein the film forming polymer is selected from an acrylate polymer, a methacrylate polymer, a urethane polymer or co-polymers thereof; and wherein the composition comprises whitening pigment in an amount of from 0.001 to 2 wt %.

Abstract: This water-in-oil emulsion-type stick-shaped deodorant composition contains: (A) a volatile component having a boiling point of 250° C. or less, where the total amount of water and ethanol in the (A) component is 83-100 mass %; (B) component (B-1), component (B-2), or a combination of components (B-1) and (B-2), wherein component (B-1) is an antiperspirant and component (B-2) is a fungicide; (C) a crosslinked silicone surfactant; (D) a non-crosslinked silicone surfactant; and (E) an oily component which has a solid phase at 25° C.

Abstract: This invention relates to oral care compositions comprising zinc phosphate, a first source of stannous (e.g., stannous fluoride); and a second source of stannous, wherein the second source of stannous comprises stannous pyrophosphate, as well as to methods of using and of making these compositions.

Abstract: Disclosed is an antimicrobial composition comprising zinc pyrithione and habit modified crystals of zinc oxide preferably comprising entrapped particles of water soluble protein. The protein may be selected from at least one of sericin, bovine serum albumin, gelatin, egg-albumin, casein, zein, whey or lysozyme. The composition may be used for personal cleansing and is especially preferred to be delivered as a shampoo or hair conditioner.

Abstract: The invention relates to an antimicrobial mixture containing 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one and an additional compound chosen from a monovalent or divalent metal salt of pyrithione, piroctone olamine, diazolidinylurea, a hexamidine compound, and imidazolidinylurea, and also to a cosmetic composition containing such a mixture. Application to caring for, making up and cleansing keratin materials.

Abstract: Disclosed is a composition comprising bisacurone. The composition finds use in treating the skin, including skin whitening applications. The composition can be obtained from an extract of turmeric rhizome.

Abstract: The present invention relates to a composition and process for reducing the drying time of solid substrate. A group of cationic surfactants in combination with low molecular weight dimethylpolysiloxanes, amodimethicones, and fatty alcohols provide for a faster water drainage.

Abstract: The present invention provides a detergent composition containing N-acyl acidic amino acids that, even at low pH, exhibits excellent solubility, has good storage stability, and creates a quality foam with satisfactory lathering performance. Specifically, the present invention provides a detergent composition and the like comprising: (A) an N-unsaturated acyl acidic amino acid wherein the unsaturated acyl is a linear acyl with 8 to 20 carbon atoms; (B) an N-saturated acyl acidic amino acid wherein the saturated acyl is a linear acyl with 8 to 14 carbon atoms; and (C) optionally, an N-saturated acyl acidic amino acid wherein the saturated acyl is a linear acyl with 16 to 20 carbon atoms; wherein the weight ratio of the component (A) to the component (B) (A/B) is 0.01 to 0.80, and the weight ratio of the component (C) to the component (B) (C/B) is 0.00 to 0.32.

Abstract: A method of formulating a personal cleansing product that will adhere to skin, includes: combining a cleansing composition with from about 18% to about 70%, by weight of the composition, of a surfactant; wherein the composition has a low shear viscosity of 100 Pa*s or more and a high shear viscosity 5 Pa*s or less; and a package with an orifice, wherein the package has a dispensing velocity of 50 cm/s or more.

Abstract: Low pH cosmetic compositions and methods for improving the appearance of skin. The low pH cosmetic compositions herein include a saccharide and, optionally, one or more additional skin care actives to improve the appearance of skin. The lower pH reduces or even eliminates some of the skin health and appearance drawbacks associated with saccharide induced glycation.

Abstract: The invention is directed to the use of at least one peptide of formula: X-(Xaa1)n-Pro*-(Xaa2)m-Y (I) With: -n=0, 1 or 2; -m=0 or 1 and if m=0 then n?0 -Xaa1 is: -An hydrophobic aminoacid selected from Alanine (Ala, A), Valine (Val, V), Methionine (Met, M), Leucine (Leu, L), Isoleucine (Ile, I), Phenylalanine (Phe, F), Proline (Pro, P) and analogues and derivatives thereof; -A polar aminoacid selected from Serine (Ser, S), Threonine (Thr, T), Tyrosine (Tyr, Y), Asparagine (Asn, N), Glutamine (Gln, Q) and analogues and derivatives thereof; -or Glycine (Gly, G); When n=2 the two aminoacids Xaa1 can be the same or different; -Xaa2 is: -An hydrophobic aminoacid selected from Alanine (Ala, A), Valine (Val, V), Methionine (Met, M), Leucine (Leu, L), Isoleucine (Ile, I), Phenylalanine (Phe, F), Proline (Pro, P) and analogues and derivatives thereof; -A basic aminoacid selected from Arginine (Arg, R), Lysine (Lys, K) and Histidine (His, H) and analogues and derivatives thereof; -Glycine (Gly, G) or Serine (Ser, S); -

Abstract: A customized skin care composition. The skin care composition includes a base composition comprising one of an aqueous alcohol composition or an aqueous emulsion. The skin care composition further includes at least two booster compositions selected from the group consisting of a first grade exfoliating agent; a second grade exfoliating agent, the second grade exfoliating agent providing greater exfoliating than the first grade exfoliating agent; a first grade whitening agent; a second grade whitening agent, the second grade whitening agent providing greater whitening than the first grade whitening agent; a first grade anti-aging agent; and a second grade anti-aging agent, the second grade anti-aging agent providing greater anti-aging effects than the first grade anti-aging agent. The base composition and the at least two booster compositions have been mixed to form a composition that is stable and has efficacious concentrations of active ingredients corresponding to skin conditions of a consumer.

Abstract: The present disclosure relates to a pump-type toothpaste composition which can be provided by being comprised in a pump-type container, and particularly, relates to a pump-type toothpaste composition with improved feeling of use when brushing teeth. In addition, the present disclosure relates to a pump toothpaste composition having improved tailing and dry-hardening property. The pump-type toothpaste composition of the present disclosure may comprise a hydrocolloid.