Formula and production method of hangover alleviating medicine

Abstract

The invention belongs to the technical field of traditional Chinese medicine preparation, and discloses a hangover alleviating medicine. The hangover alleviating medicine comprises the following raw material components by weight: 2-5g of 10-fold concentrated powder of hovenia dulcis thunb, 1-3g of 10-fold concentrated powder of radix puerariae, 10-13g of corn peptide, 0.5 g of gamma-aminobutyric acid, 0.3-0.5 g of concentrated powder of lemon powder, 0.1 g of sucralose and 3g of edible gelatin. Traditional Chinese medicinal materials such as hovenia dulcis thunb and radix puerariae and nutritional ingredients such as corn peptide and gamma-aminobutyric acid are added into the anti-alcohol medicine formula, through the synergistic effect, damage of alcohol to the liver can be relieved, metabolism and discharge of alcohol are promoted, drunkenness symptoms are relieved, body health is protected, and the formula not only can effectively dispel the effects of alcohol, but also gives consideration to the taste and stability, and has a good anti-alcohol effect. Meanwhile, no chemical medicine is adopted, all the components are pure natural traditional Chinese medicine materials, no toxic or side effect exists, all visceral organs can be comprehensively protected, and it is ensured that no extra burden is caused to the body while the effect of dispelling the effects of alcohol is achieved.

Description

Technical Field

[0001] The invention belongs to the technical field of traditional Chinese medicine pharmacy, and specifically relates to a formula of an alcohol relieving medicine and a production method thereof. Background Art

[0002] In today's society, excessive drinking is common, and the harm of alcohol to the body has attracted widespread attention. Although there are some hangover products on the market, the effect is not ideal. As a product that helps decompose alcohol and relieve the discomfort caused by alcohol, hangover medicine has a large market demand. However, while existing chemical drugs and traditional Chinese medicine preparations can help to relieve alcohol, they often put a metabolic burden on the liver and kidneys, causing secondary damage. In addition, existing hangover medicine formulas have problems such as large dosage of medicinal materials, poor effect, and incomplete organ protection.

[0003] Therefore, there is an urgent market demand and broad market prospects for developing a natural low-dose alcohol detoxification formula that has simple ingredients, small dosage, no toxic side effects on the human body, and can relieve liver and hangover. This new alcohol detoxification medicine should be able to fully protect various organs, avoid the use of large amounts of artificial vitamins, and ensure that it does not cause additional burden on the body while detoxifying. Summary of the invention

[0004] The object of the present invention is to provide a formula of a hangover relieving medicine and a production method thereof, so as to solve the problems raised in the above background technology.

[0005] In order to achieve the above-mentioned purpose, the present invention provides the following technical scheme: a formula of a hangover relieving medicine, wherein the weight ratio of the raw material components of the hangover relieving medicine includes: 2g-5g of 10-fold concentrated powder of Hovenia dulcis, 1g-3g of 10-fold concentrated powder of Puerariae lobata, 10g-13g of corn peptide, 0.5g of γ-aminobutyric acid, 0.3g-0.5g of concentrated lemon powder, 0.1g of trichlorosucrose, and 3g of edible gelatin.

[0006] Preferably, the production method of the alcohol relieving medicine comprises the following specific steps: S1, raw material preparation and weighing; S2, dry mixing and stirring: dry mixing the Hovenia dulcis concentrated powder, the Pueraria concentrated powder, the corn peptide, the γ-aminobutyric acid, the lemon concentrated powder, the sucralose, and the edible gelatin, and stirring until the raw materials are evenly dispersed; S3, sealing, sterilizing and packaging: the uniformly mixed raw materials are sealed at 10-30°C, sterilized, coded and packaged to obtain the finished products.

[0007] Preferably, the raw material preparation and weighing in S1 are specifically subdivided into: S11, Raw material selection: According to the product formula and process requirements, select high-quality Hovenia dulcis, Pueraria root, corn peptide, γ-aminobutyric acid, lemon concentrate powder, sucralose and edible gelatin; S12, raw material pretreatment: according to the characteristics of different medicinal materials, follow the principles to process the medicinal materials; S13, weighing raw materials: using precise measuring tools, weigh various raw materials according to the formula ratio.

[0008] Preferably, the preprocessing principle in S12 specifically refers to: Hovenia dulcis and Pueraria root: washing, drying and crushing to obtain Hovenia dulcis concentrated powder and Pueraria root concentrated powder; Corn peptides: Ensure that they are stored under appropriate conditions to avoid moisture and contamination; GABA: Make sure it is stored in a dry, cool, well-ventilated place, away from direct sunlight; Lemon concentrate powder: Store in a dry, cool place away from moisture and heat; Sucralose and edible gelatin: Store in a cool, dry, ventilated warehouse, avoid direct sunlight and high temperature.

[0009] Preferably, the dry mixing and stirring in S2 are specifically subdivided into: S21, dry mix; Put the weighed Hovenia dulcis concentrated powder, Pueraria lobata concentrated powder, corn peptide, γ-aminobutyric acid, lemon concentrated powder, sucralose and edible gelatin into a mixer; S22, stirring; Turn on the mixer and stir thoroughly to ensure that all raw materials are evenly dispersed without lumps; The mixing time is determined by the properties of the raw materials and the efficiency of the mixer, and usually takes 5-10 minutes.

[0010] Preferably, the sealing, sterilization and packaging in S3 are specifically subdivided into: S31, sealed; Transfer the mixed ingredients into a sealed container and make sure the container is clean and dry; Store the container in a constant temperature environment of 10-30℃, away from direct sunlight and moisture; S32, sterilization; Ultraviolet light sterilization is usually used; During the sterilization process, the temperature, time and humidity parameters must be controlled to ensure the sterilization effect. The sterilization time should be controlled within 5-10 minutes; S33, packaging and coding; Use food-safe packaging materials to package the sterilized raw materials; Put product labels and barcodes on the packaging to ensure product traceability; Store the packaged products in a dry, cool, ventilated warehouse, avoiding direct sunlight and high temperature.

[0011] The beneficial effects of the present invention are as follows: The present invention adds Chinese medicinal materials such as Hovenia dulcis, Pueraria root and other Chinese medicinal materials and nutritional ingredients such as corn peptide and gamma-aminobutyric acid into the formula of the hangover relieving medicine. Through synergistic effects, the damage of alcohol to the liver can be reduced, alcohol metabolism and excretion can be promoted, symptoms of drunkenness can be relieved, and health can be protected. At the same time, the addition of lemon powder concentrate and sucralose improves the taste and acceptance of the medicine, while edible gelatin enhances the consistency and stability of the medicine, and improves its preservation and use effects. Overall, this formula not only effectively relieves alcohol, but also takes into account the taste and stability, thus providing a guarantee for the excellent quality of the hangover relieving medicine. At the same time, the present invention does not use any chemical drugs, and all ingredients are pure natural Chinese medicinal materials, which are non-toxic and have no side effects, can fully protect various organs, avoid the use of a large amount of artificial vitamins, and ensure that no additional burden is imposed on the body while relieving alcohol. BRIEF DESCRIPTION OF THE DRAWINGS

[0012] Figure 1 The present invention is a schematic diagram of the production process of the alcohol relieving medicine. DETAILED DESCRIPTION

[0013] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0014] like Figure 1 As shown, an embodiment of the present invention provides a formula of a hangover relieving medicine, the weight ratio of the raw materials of the hangover relieving medicine includes: 2g~5g of 10 times concentrated powder of Hovenia dulcis, 1g~3g of 10 times concentrated powder of Pueraria lobata, 10g~13g of corn peptide, 0.5g of γ-aminobutyric acid, 0.3g~0.5g of concentrated lemon powder, 0.1g of trichlorosucrose, and 3g of edible gelatin.

[0015] Adding Chinese medicinal materials such as Hovenia dulcis and Pueraria root as well as nutrients such as corn peptide and γ-aminobutyric acid to the formula of hangover medicine can reduce the damage of alcohol to the liver through synergistic effects, promote alcohol metabolism and excretion, relieve symptoms of drunkenness, and protect physical health.

[0016] The production method of the alcohol relieving medicine comprises the following specific steps: S1, raw material preparation and weighing; S2, dry mixing and stirring: dry mixing the Hovenia dulcis concentrated powder, the Pueraria concentrated powder, the corn peptide, the γ-aminobutyric acid, the lemon concentrated powder, the sucralose, and the edible gelatin, and stirring until the raw materials are evenly dispersed; S3, sealing, sterilizing and packaging: the uniformly mixed raw materials are sealed at 10-30°C, sterilized, coded and packaged to obtain the finished products.

[0017] The preparation and weighing of raw materials in S1 are specifically subdivided into: S11, Raw material selection: According to the product formula and process requirements, select high-quality Hovenia dulcis, Pueraria root, corn peptide, γ-aminobutyric acid, lemon concentrate powder, sucralose and edible gelatin; When selecting Chinese medicinal materials, the origin should ensure that the medicinal materials grow in a suitable environment to ensure their efficacy and safety; the variety must comply with traditional medication habits and pharmacopoeia regulations to ensure the accuracy of the source of the medicinal materials; in terms of quality, the medicinal materials should be free of pests and diseases, impurities, and mildew, and meet the requirements for medicinal use; in terms of purity, it is necessary to ensure that there are no toxic and harmful substances and pesticide residues in the medicinal materials; the harvesting and storage methods must also be reasonable to ensure that the active ingredients and efficacy of the medicinal materials are not lost. These standards jointly ensure the quality and efficacy of Chinese medicinal materials and guarantee the safety and effectiveness of patients' medication.

[0018] S12, raw material pretreatment: according to the characteristics of different medicinal materials, follow the principles to process the medicinal materials; Medicinal material pretreatment can ensure the quality and safety of drugs. By removing impurities, improving purity, and protecting drugs from adverse factors, pretreatment provides high-quality raw materials for subsequent extraction and purification processes, while improving extraction efficiency, reducing time and energy consumption, and ensuring the safety and health of patients' medication.

[0019] S13, weighing raw materials: using precise measuring tools, weigh various raw materials according to the formula ratio.

[0020] The preprocessing principle in S12 specifically refers to: Hovenia dulcis and Pueraria root: washing, drying and crushing to obtain Hovenia dulcis concentrated powder and Pueraria root concentrated powder; Corn peptides: Ensure that they are stored under appropriate conditions to avoid moisture and contamination; GABA: Make sure it is stored in a dry, cool, well-ventilated place, away from direct sunlight; Lemon concentrate powder: Store in a dry, cool place away from moisture and heat; Sucralose and edible gelatin: Store in a cool, dry, ventilated warehouse, avoid direct sunlight and high temperature.

[0021] Among them, dry mixing and stirring in S2 are specifically subdivided into: S21, dry mix; Put the weighed Hovenia dulcis concentrated powder, Pueraria lobata concentrated powder, corn peptide, γ-aminobutyric acid, lemon concentrated powder, sucralose and edible gelatin into a mixer; S22, stirring; Turn on the mixer and stir thoroughly to ensure that all raw materials are evenly dispersed without lumps; The mixing time is determined by the properties of the raw materials and the efficiency of the mixer, and usually takes 5-10 minutes.

[0022] Among them, the sealing, sterilization and packaging in S3 are specifically subdivided into: S31, sealed; Transfer the mixed ingredients into a sealed container and make sure the container is clean and dry; Store the container in a constant temperature environment of 10-30℃, away from direct sunlight and moisture; S32, sterilization; Ultraviolet light sterilization is usually used; During the sterilization process, the temperature, time and humidity parameters must be controlled to ensure the sterilization effect. The sterilization time should be controlled within 5-10 minutes; S33, packaging and coding; Use food-safe packaging materials to package the sterilized raw materials; Put product labels and barcodes on the packaging to ensure product traceability; Store the packaged products in a dry, cool, ventilated warehouse, avoiding direct sunlight and high temperature.

[0023] It should be noted that, in this article, relational terms such as first and second, etc. are only used to distinguish one entity or operation from another entity or operation, and do not necessarily require or imply any such actual relationship or order between these entities or operations. Moreover, the terms "include", "comprise" or any other variants thereof are intended to cover non-exclusive inclusion, so that a process, method, article or device including a series of elements includes not only those elements, but also other elements not explicitly listed, or also includes elements inherent to such process, method, article or device.

[0024] Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A formula of a hangover remedy, characterized in that: The weight ratio of the raw material components of the hangover relieving medicine includes: 2g-5g of 10-fold concentrated powder of Hovenia dulcis, 1g-3g of 10-fold concentrated powder of Puerariae lobata, 10g-13g of corn peptide, 0.5g of gamma-aminobutyric acid, 0.3g-0.5g of concentrated lemon powder, 0.1g of trichlorosucrose and 3g of edible gelatin.

2. The method for producing a hangover relieving medicine according to claim 1, characterized in that: The production method of the alcohol relieving medicine specifically comprises the following steps: S1, raw material preparation and weighing; S2, dry mixing and stirring: dry mixing the Hovenia dulcis concentrated powder, the Pueraria concentrated powder, the corn peptide, the γ-aminobutyric acid, the lemon concentrated powder, the sucralose, and the edible gelatin, and stirring until the raw materials are evenly dispersed; S3, sealing, sterilizing and packaging: the uniformly mixed raw materials are sealed at 10-30°C, sterilized, coded and packaged to obtain the finished products.

3. The method for producing a hangover relieving medicine according to claim 2, characterized in that: The preparation and weighing of raw materials in S1 are specifically divided into: S11, Raw material selection: According to the product formula and process requirements, select high-quality Hovenia dulcis, Pueraria root, corn peptide, γ-aminobutyric acid, lemon concentrate powder, sucralose and edible gelatin; S12, raw material pretreatment: according to the characteristics of different medicinal materials, follow the principles to process the medicinal materials; S13, weighing raw materials: using precise measuring tools, weigh various raw materials according to the formula ratio.

4. The method for producing a hangover remedy according to claim 3, characterized in that: The preprocessing principle in S12 specifically refers to: Hovenia dulcis and Pueraria root: washing, drying and crushing to obtain Hovenia dulcis concentrated powder and Pueraria root concentrated powder; Corn peptides: Ensure that they are stored under appropriate conditions to avoid moisture and contamination; GABA: Make sure it is stored in a dry, cool, well-ventilated place, away from direct sunlight; Lemon concentrate powder: Store in a dry, cool place away from moisture and heat; Sucralose and edible gelatin: Store in a cool, dry, ventilated warehouse, avoid direct sunlight and high temperature.

5. The method for producing a hangover relieving medicine according to claim 2, characterized in that: Dry mixing and stirring in S2 are specifically divided into: S21, dry mix; Put the weighed Hovenia dulcis concentrated powder, Pueraria lobata concentrated powder, corn peptide, γ-aminobutyric acid, lemon concentrated powder, sucralose and edible gelatin into a mixer; S22, stirring; Turn on the mixer and stir thoroughly to ensure that all raw materials are evenly dispersed without lumps; The mixing time is determined by the properties of the raw materials and the efficiency of the mixer, and usually takes 5-10 minutes.

6. The method for producing a hangover relieving medicine according to claim 2, characterized in that: The sealing, sterilization and packaging in S3 are specifically divided into: S31, sealed; Transfer the mixed ingredients into a sealed container and make sure the container is clean and dry; Store the container in a constant temperature environment of 10-30℃, away from direct sunlight and moisture; S32, sterilization; Ultraviolet light sterilization is usually used; During the sterilization process, the temperature, time and humidity parameters must be controlled to ensure the sterilization effect. The sterilization time should be controlled within 5-10 minutes; S33, packaging and coding; Use food-safe packaging materials to package the sterilized raw materials; Put product labels and barcodes on the packaging to ensure product traceability; Store the packaged products in a dry, cool, ventilated warehouse, avoiding direct sunlight and high temperature.

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