Inject medicine to horse's mouth by syringe

When your horse is dyspepsia, you need feed medicine to it. But feeding medicine to horse is difficult, you need think many ideas, like add medicine to horse food, inject medicine to horse's mouth and so on.

dial a dose syringe

Inject medicine to horse's mouth by syringe. This horse syringe is common in our life, the syringe is one kind of function package. Cause the syringe is not only used to package medicine, also can inject medicine.

Now there has one kind dial a dose syringe, this syringe is easy to use for horse, This syringe has unique structure, it compose of syringe tube, plunger, tip cap, piston.locating ring. The plunger can be printed scale, and match up with locating ring can control the usage amount.

How to use the oral paste veterinary syringe?

According to the horse condition, confirm the usage amount, then rotate the locationg ring to the confirmed dosage

Insert syringe tip to horse mouth, then inject medicine

Must confirm the horse swallow the medicine

Effervescent Packaging China Manufacturer

Xinfuda group can offer customers what you need in pharmaceutical packaging area. Xinfuda as the pioneer pharmaceutical packaging manufacture in northern China. High quality, strong supply capacity and shorten shipping cycle can meet your all demand. Effervescent packaging is one set in our products.

effervescent packaging

Effervescent packaging has two series which are effervescent tablets tubes and test strip tube. The main is that desiccant cap, which can perform well in storing capsules and tablets that need dry condition. Of course, we also introduce the desiccant shelf, component of effervescent packaging and characteristics of effervescent tablets bottles. Effervescent packaging has five sizes include 84mm, 96mm, 99mm, 133mm, 144mm.

sprial desiccant cap

These can give you more choose to match your products. The raw material is PP. All the products meet the DMF and produce in CGMP standard. We will be your reliable partners in packaging.

Vitamin C effervescent tablets and packaging form

Vitamin C effervescent tablets as the name implies refers to the vitamin C through medical technology processing into effervescent tablets. Different from ordinary tablets, effervescent tablets make use of organic acid and basic carbonic acid (hydrogen) salt reaction as vesicle disintegrating agent, put into water, immediate effervescent reaction occurs, generate and release a large amount of carbon dioxide gas, like boiling, hence the name effervescent tablets.

Vitamin C for antibodies and collagen formation, tissue repair (including some REDOX function, metabolism of phenylalanine, tyrosine, folic acid, iron, carbohydrate, fat, protein synthesis, maintain immune function, hydroxyl serotonin, full blood vessels, promote the heme iron absorption and so on necessary, at the same time also has antioxidant, vitamin C fight free radicals, inhibit the formation of tyrosinase, so as to achieve whitening, pale spot effect.

vitamin c tablets packaging

Compared with ordinary, effervescent tablet agent is put into water in vitro and dissolves rapidly, releasing a large amount of carbon dioxide gas and dissolving into liquid. Generally, the disintegrating time is 1-5min. The disintegration time is 15~60min. Effervescent tablets are more easily absorbed by the body. Effervescent tablets were disintegrated and dissolved in vitro. After oral administration, the liquid was distributed in a large area of the gastrointestinal tract and absorbed into the blood through the gastrointestinal tract for about 10-30min, which reduced the local irritation of the drug in the gastrointestinal tract, thus reducing the side effects and achieving rapid and efficient effects. After oral administration, common tablets disintegrate in the stomach, slowly dissolve the drugs, and absorb them into the blood through the stomach and intestines. It takes 2~3h to reach the effective blood drug concentration, and the effect is slow.

effervescent tablet tubes

Vitamin C effervescent tablet is more strict to packing requirement, especially moisture-proof and sealing are more important. Effervescent tablet is affected by damp meeting medicine can produce metamorphism, cause to lose or reduce effect of medicine. So vitamin C effervescent piece pack chooses to contain moistureproof commonly, sealing good packing form.

effervescent tablet tubes densitometry

The density of pharmaceutical packaging materials is generally determined by the impregnation method, that is, the density is determined according to buoyancy. Impregnation law means that the buoyancy force received by the sample in the impregnation solution at a specified temperature is equal to the product of the volume of the sample displaced by the impregnation solution and the density of the impregnation solution. The buoyancy can be obtained by measuring the mass of the sample and the mass of the sample in the macerate. This method is applicable to the determination of the density of plastic containers (materials) other than foam plastics, and can be used for qualitative identification of materials.

effervescent packaging

The instrument

Scale with accuracy of 0.1mg, attached to densitometer (minimum dividing value of thermometer is 0.5°C)

Preparation and determination of test products

The test product should be placed in an environment of 23°C±2°C with relative humidity of 50%±5% for more than 4 hours, and then tested under this condition. The test product should be a task other than powder and a material without pores. The surface of the test product should be smooth, flat, no sag, clean, no crack, no air bubble and other defects. The size is suitable, and the quality of the sample should not exceed 2g.

New boiling water or other suitable liquid should be used for the macerate. The liquid that does not act with the sample can be added with lubricant if necessary, but less than 0.1% of the total volume of macerate should be used to remove small bubbles. During the test, when the test product comes into contact with the liquid, it shall have no effect on the test product. The density of macerate is generally light rain density; Water can be used when the material density is greater than 1, and anhydrous ethanol can be used when the material density is less than 1.

Desiccant cap production process

As a component of medicinal plastic bottles in pharmaceutical packaging, the production and processing of desiccant caps are similar to the requirements of the bottle body, except that the main raw material of the bottle body is blow molding grade, while the main raw material of the bottle cap is injection molding grade.

desiccant cap

The pharmaceutical bottle cap production process is:

First, feeding and batching are mainly conveyed to the hopper of the injection molding machine through pipes. After the machine is turned on, the material in the hopper enters the person's barrel to complete the process of feeding the machine.

Secondly, plasticization is a process in which the plastic batch material that enters the barrel from the hopper is heated in the barrel to reach a flowing state and has good plasticity. The requirement is that the plastic reaches the specified molding temperature before entering the mold cavity, and a sufficient amount of molten plastic is provided within the specified time.

Third, the first injection is to inject the well-plasticized melt into the mold under the pressure of the screw (injection process). When the melt is injected into the mold cavity, it passes through the nozzle, the main (sub) runner, and the gate. The resistance is very high. It has a large injection pressure loss of 30% -70%, so the process requires a sufficient injection pressure to ensure complete mold filling. This is followed by the molding stage, which consists of four steps: disposable mold, compaction, reverse flow and gate curing. The plastic melt injected into the mold cavity is cooled and shaped into a plastic cover.

Fourth, cooling and demoulding. Mainly refers to the stage from when the plastic in the gate is completely frozen to when the lid is released from the mold. Demoulding can be divided into two types: strong demolding and spin-off.

It is necessary to grasp the various production links and avoid problems before they can produce medicinal bottle caps that the customers of high quality can trust.

Effervescent Tablet Tube

The concept of the inspection result exceeding standard management was introduced for the first time, which means that the test result is beyond the legal standard and the enterprise internal control standard. Excessive inspection results do not necessarily mean that the sample inspection is not qualified. How can the effervescent tablet tube manufacturer be implemented?

effervescent packaging

First, the operating procedures for the establishment of inspection results exceeding the limits of the investigation within the company. Laboratory investigation was carried out according to the regulations to confirm whether it was laboratory bias. If it is not the laboratory deviation, the R & D, technology and production personnel should be organized to investigate the production process. It can also be interpreted as two categories: laboratory bias and non laboratory bias.

effervescent tablet tube

The laboratory deviation shall investigate any deviation of the test results caused by the factors related to the inspection process,A laboratory survey should be carried out by the professional personnel. The non laboratory deviation refers to the deviation of the test results caused by any other factors except the deviation of the laboratory. The above deviation analysis also standardizes the concrete implementation of the inspection results exceeding the standard for effervescent tablet tube factory.