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What is the role of label design for drug packaging?

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the contents printed or pasted on the drug package are collectively referred to as labels, which are divided into built-in and external. The general contents of the inner label and the outer label are the same, but there are also differences. The internal label shall contain the general name, indications or functions of the drug, specifications, usage and dosage, production date, product batch number, expiration date, manufacturer, etc. The external label shall indicate the general name, ingredients, properties, indications or functions of the drug, specifications, usage and dosage, adverse reactions, taboos, precautions, storage, production date, product batch number, validity period, approval number, production enterprise, etc
don’t worry about repetition and wordiness in the label of drug packaging. Every item of it is very important. It plays an important role in the design of drug packaging
1. Generic name of drugs: the same generic name is used for the same kind of drugs in the world, which is convenient for doctors and consumers to understand what drugs are being used and prevent the repeated use of the same kind of drugs. There are obvious differences in the printing of labels between trademarks, trade names and general drug names, which is convenient for identification
2. Ingredients: it is convenient for doctors and consumers to understand the ingredients in drugs, prevent repeated use of drugs, and prevent side effects of ingredients in different drugs and adverse effects on patients when taking other drugs
3. Properties: it is convenient for manufacturers, trading enterprises, medical institutions and consumers to understand what kind of properties normal drugs are. When drugs are contaminated or other circumstances, it is convenient for the above institutions or personnel to find problems with drugs in time
4. Indications or functional indications: it is convenient for business enterprises, doctors and consumers to understand the treatment scope of drugs and apply to diseases
5. Specification, usage and dosage: inform doctors and consumers how to take the drug. Calculate the dosage and time of taking according to the specifications<6. It has nothing to do with the possible adverse reactions of the drug or the person who should not take it carefully
7. Storage: it is convenient for manufacturers, business enterprises, medical institutions and consumers to understand the conditions under which the drug should be stored, so as to prevent changes in drug quality
8. Production date, product batch number, validity period, approval number, manufacturer and other contents: it is convenient for manufacturers, business enterprises, medical institutions and consumers to understand what enterprise the drug is produced by, whether the approved batch number is obtained after approval, and whether the product is within the validity period to ensure drug safety. It also facilitates the supervision of drug regulatory authorities and the need for enterprises to recall or regulatory authorities to control drugs in case of drug problems
9. There are also “external use signs”, “warning words” and “over-the-counter drug signs” in the label to facilitate manufacturers, trading enterprises, medical institutions and consumers to understand the nature of drugs and remind them to pay attention to storage, sales and use
the above is the significance of the label to the drug packaging design. For drugs with special requirements, the label should also pay attention to:
1. Drugs with special storage requirements should be indicated in the eye-catching position of the label
2. The period of validity in the drug label should be marked in the order of year, month and day. The year is represented by four digits and the month and day are represented by two digits. The specific marking format is “valid until XX month, XXXX” or “valid until XX month, XXXX”; It can also be expressed by numbers and other symbols as “valid until XXXX. XX.” Or “valid until XXXX /XX /XX”, etc. The period of validity of biological products for prevention shall be marked in accordance with the registration standards approved by the State Food and drug administration. The period of validity of biological products for treatment shall be calculated from the sub packaging date, and the period of validity of other drugs shall be calculated from the production date. If the validity period is marked to date, it shall be the day before the date corresponding to the starting date. If it is marked to month, it shall be the month before the month corresponding to the starting month.

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