Preparation method of a blood-nourishing oral liquid

Abstract

The present invention relates to the technical field of oral liquid production, specifically a preparation method of a blood-tonifying oral liquid, including a base, a conveying rack and a labeling unit. The upper surface of the base is fixedly connected with a conveying rack for conveying bottled blood-tonifying oral liquid. A labeling unit for labeling the bottle body of the bottled blood-tonifying oral liquid is arranged on the conveying rack. An auxiliary mechanism for position correction and auxiliary labeling of the bottled blood-tonifying oral liquid is also arranged on the conveying rack, and a reinforcing mechanism for edge reinforcement of the label on the bottled blood-tonifying oral liquid after labeling is provided. The reinforcing mechanism is arranged on the conveying rack behind the labeling unit. Through the setting of the reinforcing mechanism, the two ends of the label on the bottle body can be reinforced again after the label is attached to the bottled blood-tonifying oral liquid, avoiding the situation of warping at the two ends of the label due to the decrease in the attachment force and the insecure attachment.

Description

Technical Field

[0001] The present invention relates to the technical field of the production of blood-tonifying oral liquids, and specifically to a preparation method of a blood-tonifying oral liquid. Background Art

[0002] A blood-tonifying oral liquid is an oral preparation containing various blood-tonifying components and is commonly used to treat various anemia symptoms. The main functions of the blood-tonifying oral liquid include: supplementing iron elements, promoting the production of red blood cells, increasing the oxygen content of the blood, and alleviating anemia symptoms.

[0003] The production steps of the blood-tonifying oral liquid in the production process are as follows: First, prepare the concentrated liquid, then prepare the pectin solution, then prepare the premix, and finally make up the volume and stir the concentrated liquid, pectin solution and premix, fill and sterilize the mixed liquid, and finally use a labeling device for labeling and packaging.

[0004] When the labeling device labels the bottle body of the bottled blood-tonifying oral liquid, since the bottle body of the bottled blood-tonifying oral liquid is cylindrical, after the label is attached to the bottled blood-tonifying oral liquid, both ends of the label exceed the midline position of the bottle body. At this time, the distance between the bottle body and the labeling device will gradually increase. Therefore, the force on both ends of the label will gradually decrease during the attachment process, resulting in the situation that both ends of the label are not firmly attached. Summary of the Invention

[0005] Therefore, the present invention provides a preparation method of a blood-tonifying oral liquid, which solves the above technical problems.

[0006] The preparation method of a blood-tonifying oral liquid provided by the present invention includes the following steps:

[0007] S1. Preparation of concentrated liquid: Accurately weigh red dates, saffron, red beans, tangerine peel, and wolfberries according to the formula ratio, and obtain the concentrated liquid after processes such as crushing and pulping, heating and extraction, filtration with a filter bag, centrifugal filtration, and RO membrane concentration.

[0008] S2. Preparation of pectin solution: Add an appropriate amount of hot water at 50°C - 70°C to the mixed erythritol and completely dissolve it to obtain the pectin solution.

[0009] S3. Preparation of premix: Mix glycine ferrous, vitamin C, sodium ascorbate, vitamin B1, vitamin B2, vitamin B12, citric acid monohydrate, and sweetener evenly in a certain proportion, and then add an appropriate amount of erythritol and prepare the premix solution by the method of equal ratio dilution.

[0010] S4, constant volume stirring: the concentrated liquid obtained in S1, the pectin liquid obtained in S2, and the premix liquid obtained in S3 are uniformly mixed, and then appropriate amounts of concentrated pomegranate juice, essence, and water are added to constant volume to a fixed amount, stirred in a self-circulating manner for 3-5 minutes, and filtered through a double filter to obtain the desired blood-enriching oral liquid.

[0011] S5. Filling and sterilizing: quantitatively filling the blood-enriching oral liquid prepared in step S4 to obtain bottled blood-enriching oral liquid, and heating and sterilizing the bottled blood-enriching oral liquid at 105° C. for 30 minutes.

[0012] S6. Labeling and packaging: Use labeling equipment to label and package the sterilized bottled blood-enriching oral liquid.

[0013] The labeling equipment involved in the above-mentioned step S6 includes a base, a conveying frame and a labeling unit. The upper surface of the base is fixedly connected to the conveying frame for conveying bottled blood-enriching oral liquid, and the conveying frame is provided with a labeling unit for labeling the bottle body of the bottled blood-enriching oral liquid.

[0014] An auxiliary mechanism is used for position correction and auxiliary labeling of bottled blood-enriching oral liquid, and the conveying frame is provided with the auxiliary mechanism.

[0015] The reinforcing mechanism is used for reinforcing the edge of the label on the bottled blood-enriching oral liquid after labeling. The reinforcing mechanism is arranged on the conveying frame and at the rear side of the labeling unit.

[0016] The auxiliary mechanism includes multiple groups of L-shaped mounting frames fixedly connected to the conveyor frame and distributed front and back, each group of L-shaped mounting frames has two L-shaped mounting frames and is symmetrical left and right. The multiple L-shaped mounting frames distributed front and back are commonly provided with connecting parts, and a one-way electric push rod is fixedly connected to the vertical section of the middle group of L-shaped mounting frames, and the telescopic end of the one-way electric push rod passes through the vertical section of the L-shaped mounting frame on the left and right, and clamping parts are provided on the opposite surfaces of the two connecting parts.

[0017] The reinforcement mechanism includes a driving member arranged on the lower surface of the conveying frame. The upper surface of the conveying frame is fixedly connected to two left-right symmetrical installation frames, and fasteners are arranged on the installation frames.

[0018] According to an embodiment of the present invention, the connecting member on the right side includes a limiting guide rod that passes through the left and right sides and is slidably connected to the L-shaped mounting frames at both ends. The left ends of the limiting guide rods at both ends are commonly fixedly connected to a connecting cross plate. The middle position of the left side surface of the connecting cross plate is fixedly connected to the telescopic end of the corresponding one-way electric push rod. The front and rear ends of the left side of the connecting cross plate are fixedly connected to elastic telescopic connecting rods, and the left end of the elastic telescopic connecting rod is fixedly connected to a connecting seat.

[0019] According to an embodiment of the present invention, the clamping member on the right side includes a clamping plate fixedly connected to the left ends of two connecting seats. An installation groove is formed in the clamping plate, and an auxiliary rotating belt is rotatably connected inside the installation groove. The left and right side surfaces of the auxiliary rotating belt are flush with the left and right side surfaces of the clamping plate, and the front end of the clamping plate is provided with an outwardly curved arc surface.

[0020] According to an embodiment of the present invention, the driving member includes two symmetrically arranged mounting blocks fixedly connected to the lower surface of the conveying frame. A double-sided electric push rod is fixedly connected to the lower surfaces of the two mounting blocks, and connecting vertical plates are fixedly connected to the left and right telescopic ends of the double-sided electric push rod.

[0021] According to an embodiment of the present invention, the fastening member on the right side includes a fixed shell slidably connected inside the installation frame. The right side surface of the fixed shell is fixedly connected to the corresponding connecting vertical plate. Two left-right distributed limiting clamping plates are fixedly connected inside the fixed shell, and a plurality of fastening portions are provided on the two limiting clamping plates together.

[0022] According to an embodiment of the present invention, the fastening portion on the right side includes a pressing plate slidably connected to the two limiting clamping plates. A first connecting spring is sleeved on the outer surface of the pressing plate and located between the two limiting clamping plates. An installation cavity is formed in the left end of the pressing plate, and pressing flat plates are slidably connected through the front and rear inner walls of the installation cavity. A plurality of second connecting springs are provided between the opposite surfaces of the two pressing flat plates inside each installation cavity.

[0023] According to an embodiment of the present invention, pressing flat plates are not provided on the opposite surfaces of the two installation cavities at the front and rear ends, and the opposite surfaces of two adjacent pressing flat plates are in a fitting arrangement.

[0024] According to an embodiment of the present invention, pressing flat plates are not provided on the opposite surfaces of the two pressing plates at both ends among the plurality of pressing plates, and the opposite surfaces of two adjacent pressing flat plates are in a fitting arrangement.

[0025] Applying the technical solution of the present invention: 1. Through the setting of the reinforcement mechanism, the two ends of the label on the bottle body can be reinforced again after the bottled blood-enriching oral liquid is attached with the label, avoiding the situation that the two ends of the label are not firmly attached due to the decrease in the attachment force and resulting in warping.

[0026] 2. Through the setting of the conveying frame, the position of the bottled blood-enriching oral liquid can be corrected before attaching the label, so as to ensure that the attachment position of the label will not deviate when the bottled blood-enriching oral liquid is attached with the label, making the attachment position of the label accurate, avoiding affecting the beauty of the bottle body, and also avoiding the label being attached crookedly and resulting in insecure attachment of the label. BRIEF DESCRIPTION OF THE DRAWINGS

[0027] To more clearly illustrate the technical solutions in the embodiments of the present invention or the prior art, the following will briefly introduce the accompanying drawings required for the description of the embodiments or the prior art. Obviously, the accompanying drawings in the following description are only the embodiments of the present invention. For those of ordinary skill in the art, without creative efforts, other accompanying drawings can also be obtained based on the provided drawings.

[0028] Figure 1 It is a flowchart of the preparation method of the blood-enriching oral liquid provided by the present invention.

[0029] Figure 2 It is a three-dimensional structural schematic diagram of the labeling device in the preparation method of the blood-enriching oral liquid provided by the present invention.

[0030] Figure 3 It is a schematic diagram of the auxiliary mechanism provided by the present invention.

[0031] Figure 4 It is provided by the present invention Figure 3 An enlarged view of part A therein.

[0032] Figure 5 It is a schematic diagram of the reinforcement mechanism provided by the present invention.

[0033] Figure 6 It is a partial top view cross-sectional view of the reinforcement mechanism provided by the present invention.

[0034] Figure 7 It is a partial cross-sectional schematic diagram of the fastening part provided by the present invention.

[0035] Figure 8 It is provided by the present invention Figure 7 An enlarged view of part B therein.

[0036] Reference numerals:

[0037] 1, base; 2, conveying rack; 3, auxiliary mechanism; 4, labeling unit; 5, reinforcement mechanism; 31, L-shaped mounting frame; 32, connecting piece; 33, one-way electric push rod; 34, clamping piece; 51, driving piece; 52, fastening piece; 53, mounting frame; 321, limiting guide rod; 322, connecting cross plate; 323, elastic telescopic connecting rod; 324, connecting seat; 341, clamping plate; 342, mounting groove; 343, auxiliary rotating belt; 511, connecting vertical plate; 512, two-way electric push rod; 513, mounting block; 521, limiting clamping plate; 522, fixed shell; 523, fastening part; 5231, extrusion plate; 5232, mounting cavity; 5234, pressing flat plate. Detailed implementation manners

[0038] To make the above-mentioned objects, features, and advantages of the present invention more readily apparent, specific embodiments of the present invention are described in detail below with reference to the accompanying drawings. The following description sets forth numerous specific details to facilitate a full understanding of the present invention. However, the present invention can be implemented in many other ways than those described herein, and those skilled in the art may make similar modifications without departing from the scope of the present invention. Therefore, the present invention is not limited to the specific embodiments disclosed below.

[0039] like Figure 1 and Figure 2 As shown in the figure, a method for preparing a blood-enriching oral liquid comprises the following steps:

[0040] S1. Preparation of concentrated liquid: Red dates, saffron, red beans, orange peel, and wolfberry are accurately weighed according to the formula ratio, and the concentrated liquid is obtained after crushing and beating, heating extraction, bag filtration, centrifugal filtration, and RO membrane concentration process.

[0041] S2. Preparation of pectin solution: Add an appropriate amount of 50°C-70°C hot water to the mixed erythritol and dissolve it completely to obtain pectin solution.

[0042] S3. Premix preparation: ferrous glycinate, vitamin C, sodium ascorbate, vitamin B1, vitamin B2, vitamin B12, citric acid monohydrate, and sweetener are uniformly mixed in a certain proportion, and then appropriate amount of erythritol is added and premixed by an equal-ratio dilution method to prepare a premix liquid.

[0043] S4, constant volume stirring: the concentrated liquid obtained in S1, the pectin liquid obtained in S2, and the premix liquid obtained in S3 are uniformly mixed, and then appropriate amounts of concentrated pomegranate juice, essence, and water are added to constant volume to a fixed amount, stirred in a self-circulating manner for 3-5 minutes, and filtered through a double filter to obtain the desired blood-enriching oral liquid.

[0044] S5. Filling and sterilizing: quantitatively filling the blood-enriching oral liquid prepared in step S4 to obtain bottled blood-enriching oral liquid, and heating and sterilizing the bottled blood-enriching oral liquid at 105° C. for 30 minutes.

[0045] S6. Labeling and packaging: Use labeling equipment to label and package the sterilized bottled blood-enriching oral liquid.

[0046] The labeling equipment involved in the above-mentioned step S6 includes a base 1, a conveying frame 2 and a labeling unit 4. The upper surface of the base 1 is fixedly connected to the conveying frame 2 for conveying bottled blood-enriching oral liquid, and the conveying frame 2 is provided with a labeling unit 4 for labeling the bottle body of the bottled blood-enriching oral liquid.

[0047] The auxiliary mechanism 3 is used for position correction and auxiliary labeling of the bottled blood-enriching oral liquid. The auxiliary mechanism 3 is provided on the conveying frame 2.

[0048] The reinforcing mechanism 5 for reinforcing the edges of the labels on the bottled blood-tonifying oral liquid after labeling is provided on the conveying rack 2 and behind the labeling unit 4.

[0049] As Figure 3 shown, the auxiliary mechanism 3 includes a plurality of groups of L-shaped mounting brackets 31 fixedly connected to the conveying rack 2 and distributed front and back. The number of each group of L-shaped mounting brackets 31 is two and they are symmetrically arranged left and right. A connecting member 32 is commonly provided on the plurality of L-shaped mounting brackets 31 distributed front and back. A one-way electric push rod 33 is fixedly connected to the vertical section of the middle group of L-shaped mounting brackets 31. The telescopic end of the one-way electric push rod 33 penetrates through the vertical section of the L-shaped mounting bracket 31 left and right. Clamping members 34 are provided on the opposite surfaces of the two connecting members 32.

[0050] As Figure 3 and Figure 4 shown, taking the right connecting member 32 as an example, the right connecting member 32 includes a limiting guide rod 321 slidably connected through the L-shaped mounting brackets 31 at both ends left and right. The left ends of the limiting guide rods 321 at both ends are commonly fixedly connected with a connecting cross plate 322. The middle position of the left side surface of the connecting cross plate 322 is fixedly connected with the telescopic end of the corresponding one-way electric push rod 33. Elastic telescopic connecting rods 323 are fixedly connected to both front and rear ends of the left side surface of the connecting cross plate 322. The left end of the elastic telescopic connecting rod 323 is fixedly connected with a connecting seat 324.

[0051] As Figure 3 and Figure 4 shown, taking the right clamping member 34 as an example, the right clamping member 34 includes a clamping plate 341 fixedly connected to the left ends of the two connecting seats 324. An installation groove 342 is provided on the clamping plate 341. An auxiliary rotating belt 343 is rotatably connected inside the installation groove 342. The left and right side surfaces of the auxiliary rotating belt 343 are flush with the left and right side surfaces of the clamping plate 341. The front end of the clamping plate 341 is provided with an outwardly curved arc surface.

[0052] In specific use, when the conveying rack 2 intermittently conveys bottled blood-enriching oral liquid, first, according to the diameter of the bottle mouth of the bottled blood-enriching oral liquid, the connecting cross plate 322 is pushed by the one-way electric push rod 33, so that the clamping plate 341 approaches the bottled blood-enriching oral liquid until both auxiliary rotating belts 343 are in contact with the position of the bottle mouth of the bottled blood-enriching oral liquid. Then, the pushing of the one-way electric push rod 33 is stopped to keep the clamping plate 341 in position. At this time, the conveying rack 2 performs intermittent conveying again. Since the front end of the clamping plate 341 is bent, the bottled blood-enriching oral liquid can smoothly enter between the two clamping plates 341 along with the conveying of the conveying rack 2. When it moves to a flat position, the auxiliary rotating belt 343 will rotate inside the installation groove 342 along with the movement of the bottled blood-enriching oral liquid. At this time, the correction of the position of the bottled blood-enriching oral liquid is completed. Through the setting of the auxiliary rotating belt 343, while ensuring the smooth movement of the bottled blood-enriching oral liquid along with the conveying rack 2, the bottled blood-enriching oral liquid is kept stable during labeling. Through the setting of the elastic telescopic connecting rod 323, the elastic telescopic connecting rod 323 is telescopic. When clamping the position of the bottle mouth of the bottled blood-enriching oral liquid through the auxiliary rotating belt 343, a buffer distance can be increased, and at the same time, the fastening of the clamping of the bottle mouth of the bottled blood-enriching oral liquid can be maintained under the action of the self-elastic force of the elastic telescopic connecting rod 323.

[0053] As Figure 5 shown, the reinforcement mechanism 5 includes a driving member 51 arranged on the lower surface of the conveying rack 2. Two symmetrically arranged mounting frames 53 are fixedly connected to the upper surface of the conveying rack 2, and a fastening member 52 is arranged on the mounting frame 53.

[0054] As Figure 5 shown, the driving member 51 includes two symmetrically arranged mounting blocks 513 fixedly connected to the lower surface of the conveying rack 2. A two-way electric push rod 512 is fixedly connected to the lower surfaces of the two mounting blocks 513, and connecting vertical plates 511 are fixedly connected to the left and right telescopic ends of the two-way electric push rod 512.

[0055] As Figure 6 shown, taking the right-side fastening member 52 as an example, the right-side fastening member 52 includes a fixed shell 522 slidably connected inside the mounting frame 53. The right side surface of the fixed shell 522 is fixedly connected to the corresponding connecting vertical plate 511. Two horizontally distributed limiting clamping plates 521 are fixedly connected inside the fixed shell 522, and a plurality of fastening parts 523 are jointly arranged on the two limiting clamping plates 521.

[0056] As Figure 6 、 Figure 7 and Figure 8As shown in the figure, taking the fastening part 523 on the right side as an example, the fastening part 523 on the right side includes a pressing plate 5231 slidably connected to two limiting clamping plates 521. A first connecting spring is sleeved on the outer surface of the pressing plate 5231 and located between the two limiting clamping plates 521. An installation cavity 5232 is formed inside the left end of the pressing plate 5231. The front inner wall and the rear inner wall of the installation cavity 5232 are both slidably connected through a flat pressing plate 5234. A plurality of second connecting springs are arranged between the opposite surfaces of the two flat pressing plates 5234 inside each installation cavity 5232. The flat pressing plates 5234 are not arranged on the opposite surfaces of the two installation cavities 5232 at the front and rear ends. The opposite surfaces of two adjacent flat pressing plates 5234 are arranged in a fitting manner.

[0057] During specific use, when the bottled blood-enriching oral liquid is labeled and then moves between the two fixed shells 522 through the conveying rack 2, at this time, the conveying rack 2 stops moving. The double-acting electric push rod 512 contracts and drives the two fixed shells 522 to slide inside their corresponding installation frames 53 through the connecting vertical plate 511. At this time, the pressing plates 5231 on the two fixed shells 522 move towards each other, clamping the bottled blood-enriching oral liquid after labeling in the middle. As the double-acting electric push rod 512 continues to push, the pressing plate 5231 in contact with the bottle body of the bottled blood-enriching oral liquid receives resistance and slides towards the inside of the fixed shell 522. At this time, the first connecting spring is compressed. During the sliding process, the flat pressing plates 5234 on the pressing plates 5231 at the front and rear ends of the bottle body of the bottled blood-enriching oral liquid close to the bottle body will slide along with the bottle body and contract towards the inside of the installation cavity 5232. At this time, the second connecting spring is compressed. During the sliding process, the two ends of the label on the bottle body of the bottled blood-enriching oral liquid are pressed again, making the label adhere more firmly. Then, the double-acting electric push rod 512 returns to its original position. Under the action of the self-elastic force of the first connecting spring and the second connecting spring, the installation cavity 5232 and the flat pressing plate 5234 return to their original positions. Repeating the above steps can continuously reinforce the two ends of the label on the bottle body of the bottled blood-enriching oral liquid again. It should be noted that the movement of the double-acting electric push rod 512 moves synchronously with the intermittent movement of the conveying rack 2 and the labeling situation of the labeling unit 4. The sliding direction of the pressing plate 5231 can be kept stable through the setting of the two limiting clamping plates 521.

[0058] Working principle: In specific use, after the bottled blood-enriching oral liquid is filled, it is conveyed to the conveying rack 2. The conveying rack 2 rotates intermittently to drive the bottled blood-enriching oral liquid to move from front to back. When it moves between the two clamping members 34, the one-way electric push rod 33 pushes the clamping member 34 through the connecting member 32 to clamp the position of the bottle mouth of the bottled blood-enriching oral liquid, and cooperates with the conveying rack 2 to convey the bottled blood-enriching oral liquid. When it moves to the position of the labeling unit 4, the labeling unit 4 attaches the label to the bottle body of the bottled blood-enriching oral liquid. Then, the conveying rack 2 continues to convey the bottled blood-enriching oral liquid to the position of the reinforcement mechanism 5, and drives the fastening member 52 to slide on the mounting frame 53 through the driving member 51 to fasten both ends of the label on the bottle body of the bottled blood-enriching oral liquid.

[0059] In the description of the present invention, it should be understood that the orientation or positional relationship indicated by the terms "center", "longitudinal", "transverse", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", "axial", "radial", "circumferential", etc. is based on the orientation or positional relationship shown in the drawings, and is only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and therefore cannot be understood as a limitation of the present invention.

[0060] In addition, the terms "first", "second", "No. 1", "No. 2" are only used for descriptive purposes, and cannot be understood as indicating or implying relative importance or implicitly specifying the quantity of the indicated technical features. Thus, the features defined with "first", "second", "No. 1", "No. ②" may explicitly or implicitly include at least one such feature. In the description of the present invention, the meaning of "a plurality" is at least two, such as two, three, etc., unless otherwise specifically and clearly defined.

[0061] In the present invention, unless otherwise clearly specified and limited, the terms "installation", "connection", "connection", "fixation" and other terms should be understood in a broad sense. For example, it can be a fixed connection, a detachable connection, or integrated; it can be a mechanical connection or an electrical connection; it can be directly connected or indirectly connected through an intermediate medium, and can be the internal communication of two elements or the interaction relationship between two elements, unless otherwise clearly limited. For those of ordinary skill in the art, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

[0062] The embodiments of the specific implementation manners are all preferred embodiments of the present invention, and do not limit the protection scope of the present invention accordingly. Therefore, all equivalent changes made according to the structure, shape and principle of the present invention should be covered within the protection scope of the present invention.

Claims

1. A preparation method of a blood-enriching oral liquid, characterized in that: The following steps are involved: S1. Preparation of concentrated solution: Red dates, saffron, red beans, orange peel, and wolfberry are accurately weighed according to the formula ratio, and the concentrated solution is obtained after crushing and beating, heating extraction, bag filtration, centrifugal filtration, and RO membrane concentration process; S2. Preparation of pectin solution: Add an appropriate amount of 50°C-70°C hot water to the mixed erythritol and dissolve it completely to obtain pectin solution; S3. Premix preparation: ferrous glycinate, vitamin C, sodium ascorbate, vitamin B1, vitamin B2, vitamin B12, citric acid monohydrate, and sweetener are uniformly mixed in a certain proportion, and then an appropriate amount of erythritol is added and premixed by an equal-ratio dilution method to prepare a premix liquid; S4, constant volume stirring: the concentrated solution obtained in S1, the pectin solution obtained in S2, and the premix solution obtained in S3 are uniformly mixed, and then appropriate amounts of concentrated pomegranate juice, essence, and water are added to constant volume, stirred in a self-circulating manner for 3-5 minutes, and filtered through a double filter to obtain the desired blood-enriching oral solution; S5, filling and sterilizing: quantitatively filling the blood-enriching oral liquid prepared in step S4 to obtain bottled blood-enriching oral liquid, and heating and sterilizing the bottled blood-enriching oral liquid at 105° C. for 30 minutes; S6. Labeling and packaging: labeling and packaging the sterilized bottled blood-enriching oral liquid using labeling equipment; The labeling equipment involved in the above step S6 includes a base, a conveyor frame and a labeling unit. The upper surface of the base is fixedly connected to the conveyor frame for conveying the bottled blood-enriching oral liquid, and the conveyor frame is provided with a labeling unit for labeling the bottle of the bottled blood-enriching oral liquid. An auxiliary mechanism for position correction and auxiliary labeling of bottled blood-enriching oral liquid, the conveyor frame is provided with the auxiliary mechanism; A reinforcing mechanism for reinforcing the edge of the label on the bottled blood-enriching oral liquid after labeling, wherein the reinforcing mechanism is provided on the conveying frame and at the rear side of the labeling unit; The auxiliary mechanism includes multiple groups of L-shaped mounting frames fixedly connected to the conveyor frame and distributed front and back. Each group of L-shaped mounting frames has two L-shaped mounting frames and is symmetrical. The multiple L-shaped mounting frames distributed front and back are commonly provided with connecting members. A one-way electric push rod is fixedly connected to the vertical section of the middle group of L-shaped mounting frames. The telescopic end of the one-way electric push rod passes through the vertical section of the L-shaped mounting frame on the left and right. Clamping members are provided on the opposite surfaces of the two connecting members. The reinforcement mechanism includes a driving member arranged on the lower surface of the conveying frame, and the upper surface of the conveying frame is fixedly connected to two left-right symmetrical mounting frames, and fasteners are arranged on the mounting frames; The fastener on the right side includes a fixed shell slidably connected to the interior of the installation frame, and two limit clamps distributed left and right are fixedly connected to the interior of the fixed shell, and a plurality of fastening parts are provided on the two limit clamps; The fastening part on the right side includes an extrusion plate slidably connected to the two limit clamps, a first connecting spring is provided on the outer surface of the extrusion plate and located between the two limit clamps, an installation cavity is opened inside the left end of the extrusion plate, the front inner wall and the rear inner wall of the installation cavity are penetrated by a pressure plate slidably connected, and multiple second connecting springs are arranged between the opposite surfaces of the two pressure plates inside each installation cavity.

2. The preparation method of a blood-enriching oral liquid according to claim 1, characterized in that: The connecting piece on the right side includes a limiting guide rod that is slidably connected through the L-shaped mounting brackets at both ends from left to right. The left ends of the limiting guide rods at both ends are fixedly connected together with a connecting cross plate. The middle position of the left side surface of the connecting cross plate is fixedly connected to the telescopic end of the corresponding one-way electric push rod. Elastic telescopic connecting rods are fixedly connected to both the front and rear ends of the left side surface of the connecting cross plate, and a connecting seat is fixedly connected to the left end of the elastic telescopic connecting rod.

3. The preparation method of a blood-nourishing oral liquid according to claim 2, characterized in that: The clamping piece on the right side includes a clamping plate fixedly connected together by the left ends of two connecting seats. An installation groove is formed in the clamping plate, and an auxiliary rotating belt is rotatably connected inside the installation groove. The left and right side surfaces of the auxiliary rotating belt are flush with the left and right side surfaces of the clamping plate, and the front end of the clamping plate is provided with an outwardly curved arc surface.

4. A method for preparing a blood-enriching oral liquid according to claim 1, characterized in that: The driving piece includes two symmetrically arranged mounting blocks fixedly connected to the lower surface of the conveying frame. A two-way electric push rod is fixedly connected to the lower surfaces of the two mounting blocks together. Connecting vertical plates are fixedly connected to both the left and right telescopic ends of the two-way electric push rod.

5. The preparation method of a blood-enriching oral liquid according to claim 4, characterized in that: The right side surface of the fixed shell is fixedly connected to the corresponding connecting vertical plate.

6. A method for preparing a blood-enriching oral liquid according to claim 1, characterized in that: Flattening plates are not provided on the opposite surfaces of the two installation cavities at the front and rear ends, and the opposite surfaces of two adjacent flattening plates are arranged in a fitting manner.

Images