A degradable liquid Band-Aid, comprising the following components in parts by weight: 30-40 parts of keratin, 15-30 parts of methyl cellulose, 10-25 parts of carboxymethyl chitosan, 2-6 parts of polyvinylpyrrolidone-vinyl acetate copolymer, 0.5-1.5 parts of glycerin, 25-30 parts of ethanol, 30-40 parts of ethyl acetate, 15-25 parts of diacetone alcohol, and 20-30 parts of distilled water. Degradable keratin, methylcellulose, carboxymethyl chitosan and polyvinylpyrrolidone-vinyl acetate copolymer are used together as film-forming agents, so that a film-forming body is very elastic, has good tensile strength and is degradable.
A rapid film-forming liquid band-aid, comprising the following components in parts by weight: 10-15 parts of a polyacrylic resin, 10-25 parts of polyvinyl butyral, 7-15 parts of polyvinyl alcohol, 15-30 parts of carboxymethyl chitosan, 1-4 parts of a plasticizer, 1-3 parts of porogen, 30-40 parts of ethanol, 25-35 parts of isopropanol, 20-30 parts of diacetone alcohol, 25-40 parts of ethyl acetate, 6-20 parts of hydrogen peroxide, 2-5 parts of a Radix Notoginseng extract, 2-5 parts of a Cacumen Platycladi extract, and 25-40 parts of distilled water. The polyacrylic resin, the polyvinyl butyral, the water-soluble carboxymethyl chitosan, and the polyvinyl alcohol are used as a combined film-forming agent, thereby shortening the film forming time while ensuring that the liquid band-aid can have both flexibility and water absorption swelling.
A61L 26/00 - Chemical aspects of, or use of materials for, liquid bandages
A61L 15/22 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
A spray type liquid bandage, comprising the following components in parts by weight: 20-30 parts of ethyl cellulose, 6-10 parts of carboxymethyl chitosan, 3-5 parts of a polyvinylpyrrolidone-vinyl acetate copolymer, 15-25 parts of ethanol, 20-25 parts of ethyl acetate, 25-40 parts of diacetone alcohol, 5-15 parts of isooctane, 5-15 parts of n-hexane, 5-15 parts of n-heptane, 1-5 parts of sodium dodecyl sulfate, 1-5 parts of Tween, 0.5-1.5 parts of glycerol, and 25-35 parts of distilled water. The ethyl cellulose, carboxymethyl chitosan and polyvinylpyrrolidone-vinyl acetate copolymer are used in combination as film-forming materials, and volatile solvent combinations and volatile aid combinations are used, and sodium dodecyl sulfate and Tween are used as surface tension modifiers, so that the formed film has good flexibility and elasticity, low bonding, low surface tension and good moisture retention.
A coupled spray lid of a nasal spray bottle, comprising dual-purpose nozzle bodies (50) for placing into nasal cavities for spraying, and a cover (60) for applying a pressing force. The nozzle bodies each comprises a spray nozzle (51) and a pressing portion (53); the spray nozzles penetrate through the cover for applying the pressing force to extent into the nasal cavities for spraying; the pressing portion is used for abutting against a compression portion (32) of a suction member (30) to transmit the pressing force of the cover to the compression portion to produce a nasal spray sprayed from the spray nozzles; the cover comprises a first cover body (601) and a second cover body (602) that can be engaged with each other; when the first cover body is engaged with the second cover body, the first cover body or the second cover body is pressed to drive the two nozzle bodies to spray nasal sprays together; when the first cover body is separated from the second cover body, the first cover body or the second cover body is pressed to drive the corresponding nozzle body to spray a nasal spray. The coupled spray lid of the nasal spray bottle has a easily separatable structure, enables both simultaneous spraying for two nasal cavities and individual spraying for one single nasal cavity, is ingenious in structure and reasonable in design, and meets the actual requirements of nasal cavity caring.
A two-hole nasal cavity spray bottle capable of independent spraying, comprising a bottle chamber (10), a bottle cover (20), suction components (30), main nozzle bodies (50), and covers (60). The bottle chamber (10) comprises a chamber (14) and two independent bottle openings (13). The chamber (14) is used to store a nasal cavity spray, and the bottle openings (13) are sealedly connected to the suction components (30), the suction components (30) being used to suction out nasal cavity spray from inside the chamber (14). The main nozzle bodies (50) comprise spray heads (51), connecting panels (52), and downward pressing parts (53). The spray heads (51) and the downward pressing parts (53) are respectively arranged on opposing two sides of the connecting panels (52). The spray heads (51) penetrate through the covers (60), which exert a downward pressing force, such that the spray heads (51) extend into the nasal cavity to perform spraying. The connecting panels (52) are connected to inner surfaces of the covers (60), in order to form connecting bases for the main spray nozzle bodies (50). The downward pressing parts (53) are used to abut compression parts (32) of the suction components (30) in order to transmit the downward pressing force from the covers (60) to the compression parts (32), creating a suction movement by the suction components (30). The present spray bottle uses a structure that is easy to take apart and put back together, in order to satisfy simultaneous spraying of both nasal cavities and independent spraying or single nasal cavities.
A double-channel nasal medicament spray bottle, comprising a bottle cavity (10), a bottle cap (20), a suction component (30), a nozzle body (50) and a cover shell (60), wherein the bottle cavity (10) comprises a first chamber (16), a second chamber (17) and two independent bottlenecks (13); the first chamber (16) and the second chamber (17) are separated by means of a partition plate (15) to form two independent spaces; and the volume of the first chamber (16) is larger than that of the second chamber (17). The double-channel nasal medicament spray bottle utilizes a double-chamber design, one independent chamber, which is of a smaller volume, containing nasal medicaments, and the other independent chamber, which is of a larger volume, containing a nasal care solution or a nasal cleaning solution, so as to add other cleaning or care effects while an administration requirement is met.
A spray nozzle structure of a nasal spray bottle, comprising a spray head (51), a connecting plate (52), and a pressing part (53); the spray head (51) and the pressing part (53) are respectively disposed on two opposite surfaces of the connecting plate (52); the spray head (51) passes through a housing (60) which applies a downforce, and can extend into the nasal cavity for spraying; the connecting plate (52) is connected to the inner surface of the housing (60) to form a connection basis for a spray nozzle body (50); the connecting plate (52) is provided with a connecting part (521), a first tube opening (522), and an offset channel (523); the connecting part (521) is adapted to be connected to the inner surface of the housing (60); the first tube opening (522) is communicated with an upper suction tube (31) of a suction member (30); one end of the offset channel (523) is communicated with the first tube opening (522), and the other end of the offset channel (523) is communicated with a spray pipe (510) which passes through the spray head (51); the pressing part (53) is adapted to abut against a compression part (32) of the suction member (30) to transfer the downforce of the housing (60) to the compression part (32), forming a suction action of the suction member (30). The spray nozzle structure changes a spraying path by providing the offset channel (523), shortens the distance between two spray nozzles, and fits the two nasal cavities of the human body, thus supporting simultaneous administration or cleaning of the two nasal cavities.
A double-hole nasal spray bottle, comprising a bottle cavity (10), a bottle cap (20), a suction component (30), a nozzle body (50), and a housing (60); the bottle cavity (10) comprises at least two individual chambers (14) and two individual bottle openings (13); the chambers (14) are used for storing a nasal spray liquid; the bottle openings (13) are connected to the suction component (30) in a sealing manner; the suction component (30) is used for suctioning the nasal spray liquid from the chambers (14); the nozzle body (50) comprises spray heads (51), a connection plate (52) and pressing portions (53); the spray heads (51) and the pressing portions (53) are respectively provided on two opposite surfaces of the connection plate (52); the spray heads (51) penetrate through the housing (60) on which a pressing force is to be applied so as to enter nasal cavities for spraying. By adopting the design of the two individual chambers (14) separated from each other in a single bottle body, the spray liquid is suctioned from the two chambers (14) during one pressing process, achieving drug administration or cleaning of the two nasal cavities simultaneously, and meeting the actual needs of the nasal cleaning.
A liquid adhesive bandage, comprising the following components in percentage by weight: 10-20 parts of a main film-forming agent, i.e., ethyl cellulose, 6-15 parts of an auxiliary film-forming agent, i.e., carboxymethyl chitosan, 3-5 parts of an air-permeable modifying agent, i.e., polyvinylpyrrolidone, 1-8 parts of a plasticizer, 25-30 parts of ethanol, 30-40 parts of ethyl acetate, and 20-30 parts of distilled water. The ethyl cellulose dissolved in the ethanol and the ethyl acetate forms an isolating waterproof film on a wound. The carboxymethyl chitosan dissolved in the distilled water is inlaid in nanoscale pores of an ethyl cellulose film to form a composite film. The composite film combines the advantages of ethyl cellulose and carboxymethyl chitosan, has strong tensile strength and flexibility, is elastic, and has better antibacterial, hemostasis, healing and analgesic functions, and can promote division of epithelial cells, fibroblasts and other cells and extracellular matrix growth, thereby significantly accelerating wound healing and reducing scar formation.
A liquid adhesive bandage, comprising the following component in percentage by weight: 15-25 parts of ethyl cellulose, 10-20 parts of carboxymethyl chitosan, 5-15 parts of hydroxyethyl cellulose, 5-10 parts of hydroxypropyl methyl cellulose, 10-15 parts of a polyvinylpyrrolidone-vinyl acetate copolymer, 1-5 parts of a plasticizer, 5-15 parts of hydrogen peroxide, 30-40 parts of ethanol, 40-50 parts of ethyl acetate, 0.5-1 part of borneol, 10-15 parts of propylene glycol, and 35-60 parts of distilled water, wherein the ethyl cellulose, the carboxymethyl chitosan, the hydroxyethyl cellulose, the hydroxypropyl methyl cellulose, and the polyvinylpyrrolidone-vinyl acetate copolymer are used as a combined film-forming agent. The ethyl cellulose improves film flexibility and elasticity. The hydroxyethyl cellulose is used for improving film adhesion. The hydroxypropyl methyl cellulose, the polyvinylpyrrolidone-vinyl acetate copolymer, and the hydrogen peroxide are used in the film to form through holes for improving air permeability.
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61K 8/81 - Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
05 - Pharmaceutical, veterinary and sanitary products
Goods & Services
Disinfectants; medicines for human purposes; dietetic foods
adapted for medical purposes; depuratives; veterinary
preparations; preparations for destroying noxious animals;
dressings, medical.
Dental apparatus and instruments; medical apparatus and
instruments; ice bags for medical purposes; physiotherapy
apparatus; cooling patches for medical purposes; feeding
bottles; contraceptives, non-chemical; orthopedic articles;
suture materials.
Medical apparatus and instruments; corn knives; massage
apparatus; temperature indicator labels for medical
purposes; therapeutic facial masks; ophthalmoscopes;
surgical apparatus and instruments; radiological apparatus
for medical purposes; dental apparatus and instruments;
gloves for medical purposes; belts for medical purposes;
cushions for medical purposes; ice bags for medical
purposes; masks for use by medical personnel; cooling
patches for medical purposes; sanitary masks for medical
purposes; feeding bottles; contraceptives, non-chemical;
surgical implants comprised of artificial materials;
abdominal belts; orthopaedic articles; suture materials;
thermometers for medical purposes.
05 - Pharmaceutical, veterinary and sanitary products
Goods & Services
Veterinary preparations; preparations for destroying noxious
animals; dressings, medical; disinfectants; medicines for
human purposes; dietetic foods adapted for medical purposes;
depuratives.
Disclosed is a self-destructing safety needle sleeve. The needle sleeve comprises: a needle sleeve body (1), in which an accommodation groove (2) capable of accommodating a needle tube is provided, and a front end of which is provided with an opening part (3) in communication with the accommodation groove (2); a needle fixing part (4), on which a fixing hole (401) used for being sleeved and fixed to a needle (A) is provided; an adhesive capsule (5), which is a capsule structure wrapping around an adhesive therein and is provided at a tail end of the accommodation groove (2); and an adhesive capsule support (6), which is a lever structure provided in the accommodation groove (2), wherein a support point (601) of the lever structure is provided at the bottom part of the accommodation groove (2), an end, close to the opening part (3), of the lever structure is provided with a protruding needle peduncle holder (602), and the adhesive capsule (5) is fixed to the other end of the lever structure. By means of the self-destructing safety needle sleeve, the needle can be effectively prevented from loosening, and the needle can be protected even if the loosening of the needle occurs, thereby avoiding the needle from being exposed and causing secondary damage.
A61M 5/32 - NeedlesDetails of needles pertaining to their connection with syringe or hubAccessories for bringing the needle into, or holding the needle on, the bodyDevices for protection of needles
A motion sickness sticker attached to eyes, including a sequentially set backing layer, ointment layer and protective layer, wherein an adhesive layer is provided at both ends or around the inside of the backing layer; and the ointment layer is placed on the inner middle portion of the backing layer. The ointment layer comprises: 2-3 parts of Ziziphi Spinosae Semen, 3-5 parts of menthol, 1-2 parts of Borneolum Syntheticum, 0.5-1 parts of Moschus, 2-3 parts of Salviae Miltiorrhizae Radix et Rhizoma, 2-3 parts of Phellodendri Amurensis Cortex, 0.2-0.5 parts of lemon essential oil, 1-2 parts of Allii Sativi Bulbus, 1-2 parts of jojoba oil, 2-3 parts of lotus plumule powder, 3-6 parts of Zingiberis Rhizoma Recens, 15-30 parts of a humectant, 5-15 parts of a gelatinizer, and 0-20 parts of a skin care agent.
The present invention relates to the field of daily chemicals, and relates in particular to an alcohol-free bacteriostatic Florida water and a preparation method therefor. The alcohol-free bacteriostatic Florida water comprises Sophora flavescens extract, Rehmannia glutinosa extract, propolis extract and a concentrated liquid obtained after soaking Sophora flavescens, Rehmannia glutinosa, propolis and Polygonatum sibiricum in ethanol and then removing the ethanol; the addition of Polygonatum sibiricum increases the dissolution rates of the active ingredients of Sophora flavescens, Rehmannia glutinosa and propolisin in the ethanol, and improves the effectiveness of the Florida water in heat clearing and detoxification, swelling reduction and pain relief, and bacteria sterilization. Meanwhile, a soaking liquid mixture of Sophora flavescens-Rehmannia glutinosa-propolis-Polygonatum sibiricum synergisitically cooperates with a water extract of ophora flavescens, Rehmannia glutinosa and propolis to enhance the self-defense capabilities as well as the adaptability to various active ingredients of the skin, which is beneficial in improving the adsorptivity of functional ingredients on the surface of the skin such that the pharmaceutical effect lasts longer. Meanwhile, the Florida water does not contain ethanol, making the Florida water safer to use. The present invention organically combines the soaking and water extraction processes, which greatly improves the dissolution rate of each active ingredient, and achieves extremely high efficacy.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/98 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution of animal origin
A61Q 13/00 - Formulations or additives for perfume preparations
A61Q 17/02 - Barrier preparationsPreparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
Disclosed by the present invention is a mask, comprising a mask face and ear-hook portions detachably connected to left and right ends of the mask face, wherein the mask face comprises a first conductive mesh layer, an insulating and breathable layer and a second conductive mesh layer which are successively attached from the outside to the inside; the first conductive mesh layer is electrically connected to the positive electrode of a power supply device, and the second conductive mesh layer is electrically connected to the negative electrode of the power supply device; end portions extending toward the back of a human cheek are formed on left and right ends of the mask face, and an interface of the power supply device is provided near the end portions; the ear-hook portions comprise a ring-shaped ear hook and an extension segment which are arranged in order along the extension direction of the end portions; the front ends of the ring-shaped ear hooks are connected to the end portions, and the ends thereof are integrally formed with the extension segments. The present mask may improve sealing tightness and avoid ear pain caused by long-term wearing.
Provided is a real-time monitoring smart fever-reduction sticker, comprising a fever reduction sticker body, a temperature sensing module, a temperature display module, and a control module; the fever reduction sticker body comprises a carrier and a semiconductor fever reduction layer located on the carrier; a protective layer is attached to the upper surface of the semiconductor fever reduction layer; the temperature display module is attached to the upper surface of the protective layer; a thermally conductive layer and a contact layer are attached, in sequence from top to bottom, to the lower surface of the semiconductor fever reduction layer; the temperature sensing module is located between the thermally conductive layer and the contact layer; the temperature sensing module can obtain the temperature of the forehead of a patient in real time.
A medical antipyretic patch comprises an antipyretic patch member (1) and a fixing sleeve (2). The antipyretic paste member (1) comprises a backing layer (10), a gel layer (12), and a protective film layer (13) disposed in sequence. A rear surface of the backing layer (10) is provided with a ring-shaped adhesive female fastener (14). The fixing sleeve (2) comprises a sleeve member (3), a fixing strap (4) connected to the sleeve member (3), and a locking component (5) provided on the fixing strap (4). An inner layer of the sleeve member (3) is provided with a ring-shaped adhesive male fastener (6) corresponding to the adhesive female fastener (14). The antipyretic patch firmly fixes the antipyretic patch member (1) to multiple parts of a patient's body, thereby preventing the antipyretic paste member (1) from detaching from an patched part due to movement of a patient during use and ensuring an antipyretic effect. The gel layer (12) of the antipyretic patch has a good antipyretic effect, a pleasent aroma, and a strong soothing effect, thereby facilitating an antipyretic treatment for a patient. The antipyretic paste is easy and comfortable to use, has a good antipyretic effects, and has good promotion and application prospects.
An automatic skin wound recognition-based medicine recommendation method, comprising the steps of: skin wound image acquisition (S1), a skin wound image at least comprising therein front image information about a skin wound of a patient; wound contour feature extraction (S2), to obtain a wound feature of the skin wound image; wound feature recognition (S3), importing the wound feature into a wound feature matching library for similarity matching, so as to recognize the type of the skin wound of the patient; and medicine recommendation (S6), performing indexing according to the type of skin wound of the patient, so as to obtain a medicine list suitable for the type of the skin wound of the patient, and pushing the medicine list to a mobile terminal. The method above performs medicine recommendation in an automatic skin wound recognition method, eliminating a buyer consultation process, lowering requirements on salesclerks, providing a basis for new retails of medicines for external use, such as for skin.
An infrared magnetic therapeutic patch, comprising a nonwoven adhesive tape, an infrared compound medicinal material layer coated on the nonwoven adhesive tape, and a protective film used for protecting the infrared compound medicinal material layer, also comprising permanently magnetized pieces, the permanently magnetized pieces being arranged and joined into a right-angled whirling channel, and the infrared compound medicinal material layer being filled in the whirling channel. The energy-absorbing effect of the infrared compound medicinal material layer is increased, magnetic force uniformity and a broadened range are ensured at the same time, and infrared magnetic therapeutic effects are increased.
Provided is a medical far-infrared magnetic therapy patch, comprising: a fixing sleeve (1) and a far-infrared magnetic therapy patch body (2) detachably provided on the fixing sleeve (1); the far-infrared magnetic therapy patch body (2) comprises a backing layer (20), a magnetic sheet (22), and a protective film (23) arranged in order; a lug (24) is provided on the side of the backing layer (20); the fixing sleeve (1) comprises a sleeve body (3), a fixing belt (4) connected to the sleeve body (3), and a locking member (5) provided on the fixing belt (4). The present solution can promote blood circulation, activate biological cells, and strengthen cell tissue regeneration capacity through magnetic therapy, and help the growth of biological enzymes, exert the metabolic function of the body, such that the effects of warming and removing cold, removing wind and dampness, reducing swelling and pain, repairing tissue damage, and treating and regulating autonomic disorders are achieved. The present solution can firmly fix the far-infrared magnetic therapy patch body on multiple parts of the body of the patient, which can prevent the far-infrared magnetic therapy patch body from separating the application site due to patient movement during use, and ensure the effect of magnetic therapy.
A medical skin treatment device comprises: a housing (1), a cylinder (11) being provided on a base of the housing (1); a packer (2), wherein the packer (2) is provided at an upper portion of the cylinder (11), the packer (2) is fixedly connected to a movable portion of the cylinder (11), a driving motor (21) is provided at a central axis of the packer (2), multiple packing units (22) are provided at the periphery of an inner wall of the packer (2), the packing units (22) are connected to a main shaft of the driving motor (21) by a radiation wall structure (23), the top of the packing units (22) comprise a material feeding module (221), and the material feeding module (221) is in the shape of a syringe barrel; a mixer (3) internally provided with a cavity for mixing fillers, the mixer (3) being provided with a receiving module (31), and the receiving module (31) matching the material feeding module (221); and a mask (4), one end of the mask (4) communicating with the mixer (3) via a guide tube (5). The medical skin treatment device automatically prepares a treatment medicament, and an ingredient ratio thereof is precise and adjustable, thereby facilitating facial treatments.
A far infrared magnetic therapy patch, comprising a substrate layer (1), a drug layer (2), a magnetic sheet layer (3), a protective film layer (4), and an anti-stick layer (5), wherein the magnetic sheet layer (3) is made out of a sintered neodymium-iron-boron permanent magnet material and a remnant flux density of 70-130 mT. A far infrared physiotherapy block (6) can emit far infrared rays having a wavelength of 9-15 μm and being capable of penetrating through skins and subcutaneous tissue to achieve the effects of acupuncture therapy and needling. When the far infrared physiotherapy block (6) is combined with a magnetic sheet and a Traditional Chinese Medicine prescription, the efficacy of Traditional Chinese Medicines has an effect on meridians and acupoints by means of human skins using far infrared heat and magnetic induction methods to facilitate and improve blood circulation and lymph circulation, thereby producing an analgesia effect, an apocatastasis effect, etc., and achieving the effect of alleviating and suppressing pains caused by the diseases above.
An anti-inflammatory and antimicrobial ointment comprises a component A and a secondary component B. The component A comprises the following ingredients in parts by weight: 15-30 parts of a sicklepod extract; 10-20 parts of a ginkgo seed extract; 5-9 parts of a Sichuan pepper extract; 2-6 parts of a champac extract; 2-7 parts of konjac glucomannan; and 1-3 parts of chitosan oligosaccharide. The secondary component B comprises: 1-3 parts of zein; 1-3 parts of glycerol; and 0.3-1 parts of beeswax. The anti-inflammatory and antimicrobial ointment achieves moderate yet significant and long-lasting anti-inflammatory and antimicrobial effects. When applied to infected skin, such as a pustule, superficial wound infection, or eczema with bacterial infection, or a surface of a purulent wound with discharge, the ointment forms a protective thin film, thereby achieving robust anti-inflammatory and antimicrobial effects, and facilitating healing of a wound surface.
Provided is a TCM gel or ointment for treating allergic rhinitis, comprising the following components in parts by weight: 8-10 parts of Artemisia argyi extract, 4-6 parts of honeysuckle extract,; 2-4 parts of mint extract, 3-8 parts of Glycyrrhiza uralensis extract, 70-75 parts of medical gel, and 5-7 parts of double distilled water. Said TCM gel or ointment can be used for nasal congestion, and can relieve symptoms such as nasal obstruction, running nose, sneezing, and the like.
Disclosed is a long-acting sustained-release traditional Chinese medicine cold compress for treating skin ulcers, comprising, in parts by weight, 10-25 parts of orange peels, 10-20 parts of willow branch bark, 10-20 parts of docynia delavayi, 5-17 parts of barley bran, 5-15 parts of cocklebur fruit, 3-15 parts of Caenopteris japonica, 3-15 parts of concha haliotidis, 1-2.5 parts of calcined oyster and 1-2 parts of cortex hibisci bark. The traditional Chinese medicine cold compress can continuously and stably release active ingredients of the traditional Chinese medicine into an ulcer lesion without causing secondary injury to the wound due to wound adhesion, and the matrix of the traditional Chinese medicine cold compress maintains a wet environment on the ulcer surface, thus being capable of promoting healing of the ulcer.
A61K 47/44 - Oils, fats or waxes according to two or more groups of Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
Provided is a burn/scald spray for accelerating wound healing, comprising the following raw materials in parts by weight: 5-15 parts of chenpi, 5-10 parts of Salicis cortex, 3-9 parts of Docynia delavayi, 3-9 parts of Eucalyptus robusta, 2-7 parts of Chestnut leaves, 1-5 parts of Glycyrrhizy uralensis, 1-3 parts of Concha haliotidis, 0.5-2.2 parts of Concha Ostreae, 0.2-1.8 parts of black bean, and 1-2 parts of maize bran.
A Chinese medicinal herbal skin cream for treating rhagades of hands and feet, comprising the following components in parts by weight: 6-8 parts of rhizoma bletillae extract, 4-6 parts of Fructus meliae azedarach extract; 2-4 parts of aloe extract, 10-15 parts of glycerol, and 55-60 parts of ointment auxiliary material. The Chinese medicinal herbal skin cream is applied to skin with rhagades. The skin cream is mild without irritation, and can effectively heal cracks, exfoliate, simulate epithelial hyperplasia, and alleviate or relieve pain.
Disclosed is a TCM ointment for treating allergic dermatitis, consisting of 6-8 parts of Artemisia argyi extract, 4-6 parts of radix Sophora flavescens extract, 2-4 parts of sesame extract, 2-4 parts of Tuber fleeceflower extract, 10-15 parts of pearl powder, and 55-60 parts of ointment excipient. Said ointment can relieve affected skin area, such as erythema, swelling, papule, and the like.
Provided is a TCM patch for softening scars, comprising the following raw materials in parts by weight: 10-20 parts of chenpi, 10-15 parts of common clubmoss herb, 10-15 parts of eggplant peel, 5-12 parts of Ramulus Mori, 5-12 parts of chestnut leaves, 3-10 parts of Docynia delavayi, 3-8 parts of Concha haliotidis, 1.5-5 parts of Gleditsia sinensis, 1.5-5 parts of Concha Ostreae, and 1-3 parts of Shrubalthea Bark. Said TCM patch may soften scars, dredge Qi and blood, remove turbid Qi, and repair partially damaged skin.
A61K 36/00 - Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
A61K 35/56 - Materials from animals other than mammals
Provided is a skin care gel containing natural extracts, comprising (in parts by weight): 20-30 parts of a carbomer gel, 4-5 parts of glycerin, 2-3 parts of hyaluronic acid, 10-20 parts of distilled water, 0.1-0.2 parts of a Blumea megacephala extract, 0.1-0.2 parts of an Artemisia argyi extract, and 0.1-0.2 parts of a peppermint extract. The skin care gel effectively improves anti-pruritic and anti-allergic effects by the addition of Chinese herbal extracts.
A61K 8/81 - Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
A61K 8/02 - Cosmetics or similar toiletry preparations characterised by special physical form
A61K 8/98 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution of animal origin
Disclosed is an anti-bacterial and anti-inflammatory mouthwash, mainly composed of deionized water, and at least added to with a combination of a tranexamic acid, chlorogenic acid, Andrographis paniculata extract and honeysuckle extract. By using means of combining the chlorogenic acid, Andrographis paniculata extract and honeysuckle extract with tranexamic acid, the mouthwash has the functions of anti-inflammation, rapid prevention of gum bleeding and effective inhibition of oral bacteria, so as toachieve the purpose of treating the symptoms and the causes.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/44 - Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfurSalts, esters or N-acylated derivatives thereof
Provided is an emollient oil for preventing mosquito bites, wherein an essential oil with comparatively good skin compatibility is used as the main ingredient, and mosquito repelling ingredients with functional effects and active components for promoting the activity of the mosquito repelling ingredients are added at the same time, so that the resulting emollient oil can be well adsorbed on the skin surface and has mosquito repelling effects.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/92 - Oils, fats or waxesDerivatives thereof, e.g. hydrogenation products
A61Q 17/02 - Barrier preparationsPreparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
Provided is a mosquito repellent spray for a skin surface, wherein an essential oil with comparatively good skin compatibility is used as the main ingredient, and mosquito repelling ingredients with functional effects and active components for promoting the activity of the mosquito repelling ingredients are added at the same time, so that the resulting spray can be well adsorbed on the skin surface and has mosquito repelling effects.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/92 - Oils, fats or waxesDerivatives thereof, e.g. hydrogenation products
A61Q 17/02 - Barrier preparationsPreparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
Disclosed is an anti-mosquito emulsion, comprising the following ingredients (by mass fraction): ingredient A: linalool: citronellol: geraniol 1: 1: 1: to 1: 2: 2; ingredient B: essential oil of Artemsia argyi; ingredient C: 2 to 5 parts of lecithin, 0.001 to 0.1 part of ephedrine, 0.5 to 1 part of poria cocos extract, 2 to 10 parts of natural squalane, 1 to 5 parts of VE or VE derivative; ingredient D: 8 to 18 parts of glycerol; the balance is water; wherein the ingredient A and ingredient B are mixed homogeneously at a ratio of 1: 4 to 2: 3; when the ingredient C and the ingredient D are mixed homogeneously, the mixture of the ingredient A and the ingredient B is added, and then 6 to 12 parts of emulsifier, 0.2 to 0.5 part of surfactant and 3.8 to 10 parts of consistency regulator are added; the mixture of ingredient A and ingredient B : the mixture of ingredient C and ingredient D is 1: 5 to 2: 5. The emulsion uses an essential oil having good compatibility with the skin to wrap about anti-mosquito ingredients to form an adsorption layer having better compatibility with the skin, so that the prepared anti-mosquito emulsion is more suitable for the surface of the skin.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/92 - Oils, fats or waxesDerivatives thereof, e.g. hydrogenation products
A61Q 17/02 - Barrier preparationsPreparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
Disclosed is an anti-acne traditional Chinese medicinal ointment, comprising the following ingredients: an aloe water extract; a ginseng water extract; a honeysuckle water extract; a wild chrysanthemum water extract; a dandelion water extract; a purslane water extract; vitamin E; vitamin B5; a butanediol; a superoxide dismutase; a 5-ureidoacelolactam; and deionized water. The ointment can suppress Bacterioides, balance oil secretion, clear skin waste and toxins, and eliminate inflammations.
A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
A61K 31/047 - Hydroxy compounds, e.g. alcoholsSalts thereof, e.g. alcoholates having two or more hydroxy groups, e.g. sorbitol
Provided is a long-acting bacteriostatic mouthwash, comprising a combination of a Phellodendron amurense extract, a Herba Artemisiae Scopariae extract, common Andrographis herb and a European Verbena herb extract, wherein deionized water serves as the main ingredient. The mouthwash can prevent gingival bleeding and inhibit oral bacteria.
Provided are a bacteriostatic hand lotion and a preparation method therefor. The hand lotion contains 15-18 parts of Coptis chinensis, 20-23 parts of a peppermint oil, 2-4 parts of Scutellaria baicalensis, 2-4 parts of Folium isatidis, 5-8 parts of an Artemisia argyi essential oil, 2-5 parts of Rhizoma anemarrhenae, 10-13 parts of a dandelion essential oil, 2-4.5 parts of a VE derivative, 6-10 parts of an emulsifier, 0.2-0.5 parts of a surfactant, and 3.8-6 parts of a consistency regulator, and the balance is deionized water.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/92 - Oils, fats or waxesDerivatives thereof, e.g. hydrogenation products
A61Q 17/00 - Barrier preparationsPreparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
Provided is a skin toner containing a Calendula officinalis extract, comprising the following raw materials (in parts by weight): 10-30 parts of a Calendula officinalis extracting solution, 6-12 parts of hyaluronic acid, 2-10 parts of silk hydrolyzate, 2-9 parts of rose hip oil, 1-10 parts of glycerol, and 30-50 parts of water. The skin toner can rapidly replenish moisture for the skin, equilibrate oils, prevent pigmentation, improve skin radiance and elasticity, slow down skin aging, and prevent skin laxity and wrinkles.
A61K 8/98 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution of animal origin
Provided is a traditional Chinese medicine skin cream, comprising the following raw materials in parts by weight: 15-28 parts of a walnut meal extract, 2-18 parts of a Dendrobium officinale extracting solution, 0.3-1.5 parts of a lavender essential oil, 3-15 parts of a Rhodiola rosea extract, 5-10 parts of a rose hip oil, 10-20 parts of pearl powder, and 10-30 parts of ointment excipients. Long-term use can make the skin stay white, tender and moisturised.
A61K 8/92 - Oils, fats or waxesDerivatives thereof, e.g. hydrogenation products
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 8/98 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution of animal origin
Disclosed is a long-acting mosquito repellent containing extracts of traditional Chinese medicines. A main component of the long-acting mosquito repellent is deionized water. A combination of an extract of artemisia leaves, an extract of cloves, peppermint essential oil and an extract of agastache is at least added into the long-acting mosquito repellent. The long-acting mosquito repellent also comprises an extract of purple perilla, or a combination of the extract of purple perilla and an extract of calamus or a combination of the extract of purple perilla, the extract of calamus and an extract of eupatorium.
A skin care glycerol containing Chinese herbal extracts, comprising: 40-50 parts by weight of glycerol, 1-2 parts by weight of vaseline, 0.5-1 parts by weight of sodium dodecyl sulfate, 5-10 parts by weight of ethanol, 20-30 parts by weight of distilled water, 0.2-0.3 parts by weight of a Herba schizonepetae extract, and 0.2-0.3 parts by weight of a Radix angelicae dahuricae extract. The skin care glycerol is antipruritic and antiallergic, is mild and non-irritating to the human skin, and is suitable for infants.
A61K 8/97 - Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from algae, fungi, lichens or plantsCosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof, of undetermined constitution from derivatives thereof
A61K 47/44 - Oils, fats or waxes according to two or more groups of Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
A61K 47/20 - Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
An antibacterial and tooth protection gargle, using deionized water as the main ingredient, and comprising at least a combination of magnolol, a Rhizoma anemarrhenae extract, a Herba andrographitis extract, and a Radix et rhizoma rhei extract. The gargle can quickly diminish inflammation and prevent gum bleeding, thereby effectively inhibiting oral bacteria.
A traditional Chinese ointment for external application for anti-inflammation and swelling relief, consisting of the following components in parts by weight: 15-20 parts of seeds of Fructus hippophae, 10-15 parts of Cortex phellodendri, 8-12 parts of Radix rehmanniae, 8-12 parts of Cota tinctoria, 5-15 parts of Fructus forsythiae, 5-15 parts of Ramulus uncariae cum uncis, 5-10 parts of pumpkin seed, 3-7 parts of Ligusticum chuanxiong, 3-5 parts of VB5, and 3-5 parts of transdermal enhancer. The transdermal enhancer comprises 30-40 wt% of menthol, 30-40 wt% of Borneolum syntheticum, 15-20 wt% of PEG, and 10-15 wt% of octanol.
An ointment for rapidly repairing surfaces of burn and scald wounds comprises: 18 to 20 parts of petroleum jelly, 8 to 12 parts of glycerol, 1 to 2 parts of allantoin, 15 to 25 parts of glyceryl stearate, 0.5 to 1 part of camellia oil, 10 to 20 parts of distilled water, 0.1 to 0.2 parts of extract of hooked spikemoss, 0.1 to 0.2 parts of extract of Chinese ilex barks, and 0.1 to 0.2 parts of extract of gromwell by weight.
A61K 36/00 - Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
A61P 17/02 - Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
50.
ANTIBACTERIAL AND ANTIPRURITIC TRADITIONAL CHINESE OINTMENT AND PREPARATION METHOD THEREFOR
An antibacterial and antipruritic traditional Chinese ointment, comprising the following components: 50 wt% of a Radix stemonae ethanol-water extract, 50 wt% of a Radix sophorae flavescentis ethanol-water extract, a chlorhexidine acetate, a Flos lonicerae extract, a Herba taraxaci extract, a Herba menthae extract, Borneolum syntheticum, polyethylene glycol, glycerinum, menthol, and disodium lauryl amphoacetate. The traditional Chinese ointment can be used for treating dermatitis.
