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The Decision 323/byt-Qđ Issued Regulation: The Information, Advertising Drugs And Cosmetics For Men

Original Language Title: Quyết định 322/BYT-QĐ: Ban hành Quy chế thông tin, quảng cáo thuốc và mỹ phẩm dùng cho người

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ĐỊNHVề DECISION decision issuing "information regulation, tobacco and cosmetics ads for the" Health Charter for TẾCăn smoking rooms, healing attached to Decree No. 24 dated 23/1/1991 of the Council of Ministers (Government);
Pursuant to Decree No. 68/CP dated 11/10/1993 of the Government functions, tasks, powers and organization of the Ministry of health;
Pursuant to Decree No. 194/CP of the Government on 31/12/1994 on ad operations on the territory of Vietnam;
At the suggestion of the Director of the Vietnam pharmaceutical Management Bureau;
 RESOLUTION ĐỊNHĐiều 1. Attached to this decision "information regulation, advertising drugs and cosmetics for people". 2. This regulation is effective from 1/3/1997 replace "regulation of drug information and healing for people" issued by decision of the Minister of health no. 646/BYTQĐ on 16/8/1993.
Article 3. He (she) Chief, Director of the Vietnam drug administration, Director of the treatment, the Chief Inspector of the Ministry of health, General Director of Vietnam Pharmaceutical Corporation, Director of the provincial health department, central cities and health departments, the heads of the units directly under the Department of health is responsible for implementation of this decision., INFORMATION and REGULATION of DRUG ADVERTISING , COSMETICS for MEN (attached to decision No. 322/BYTQĐ, 28/2/1997 of the Minister of health) this regulation specifies the rules and procedures of information and advertising of medicines, cosmetics for men have been allowed to circulate.
 Chapter I: information, DRUG ADS for PEOPLE I. CHUNGĐiều RULES 1. Smoking prevention and cure for the special goods, directly affect the health and life of people sick, so information, drug ads are aimed at making the physician and the user have the correct understanding of the nature, effects and how to use the drug to use reasonable the safe, consistent with national policy of Vietnam issued under resolution No. 38/CP dated 20/6/1996 of Government. 2. All information, advertising on smoking for people to ensure objectivity, accuracy, honesty, science, apparently.
Article 3. The unit or individual is allowed to operate information, drug ads and those who directly provide information, drug ads are responsible for the content of information, advertising and other activities.
 
II. information THUỐCĐiều 4. Drug information stipulated in this regulation is the activity that provides information about drugs used for people of the Organization, individuals are responsible for drug information. Drug information to meet the information requirements of the facilities, individuals are direct medical practice, pharmacy or users. Article 5. The Ministry of health, Department of health, health departments, units and individuals to practice medicine, pharmacy participating organizations are responsible for the activities of information about smoking in the range of occupations in the unit, the individual management.
Article 6. Only be offers information on smoking was the Ministry of health for permission or information is full of scientific facts have been verified; must clearly indicate the source of the information, the person providing the information, the time of providing the information.
Article 7. Just received official information about the drug organization and individual are allowed to provide information about the drug or the information according to the report template has been defined.
 
III. AD THUỐCĐiều 8. Drug advertising provisions in this regulation is the introduction of operations by drug manufacturers, drug business conducting or funding to strengthen the prescription, supply, sale and consumption of drugs, on the basis of rational drug use, safety. 9. The active form of the drug ads: 1. Drug ads for health officials: through "people introduce drugs" released brochures smoking workshops introduce the drug exhibits, introducing smoking conferences, seminars for medical cadres.
Funding for conferences in the medical industry.
2. Drug ads to the public: On books, newspapers, magazines, brochures left.
On the medium of television.
On radio media.
Through the fair, the exhibition On the mass media.
Article 10. All information in the operation of a drug product ads must conform to the following documents: 1. Summarizing the characteristics of products certified by the Ministry of health (or equivalent governing body) of the country, which allows drug production and circulation.
2. documents of registration of medicine has been the Ministry of health (the Vietnam pharmaceutical Management Bureau) issued the registration number.
Article 11. Prohibit the following acts: 1. Use of material or financial benefits in any form to affect physician, pharmacist in the sale, purchase, prescription drugs.
2. Use the number sign allows a circulation of drugs of the Ministry of health (the Vietnam pharmaceutical Management Bureau), the name and position of the medical officers, the type of correspondence, results of clinical studies have not yet allowed the Ministry of health, the Scientific Conference to operate drug ads.
 
CATEGORY A: DRUG ADS for medical STAFF. Article 12:1 drug ads for medical officers defined in this regulation is the advertising activities for the physician, pharmacist, health officials are directly related to smoking.
2 words, picture taking drug ads for medical officers must fit the facts of science has been admitting about smoking; medication name nomenclature used by Vietnam Pharmacopoeia, name the disease according to French Medical Dictionary Encyclopedia or dictionary English medical Encyclopedia.
Article 13: the content of drug advertising for medical officers include the following information: the name of the drug: the name miscellaneous (by the manufacturer)-Copyright International Name (INN) or the original name (generic name) name of active ingredient: called follow the international nomenclature does not have copyright (INN) or the original name (generic name).
Dosage dosage formulation specifies the use and side effects harmful reaction and things to the interaction of the drug name and address of the manufacturer, buy sell smoking materials were used to consult the article 14: "The introduction of the drug" represents the production base drug trading is allowed to operate legally on the territory of Vietnam and must have the following criteria: 1. The pharmacist, or physician, or health care salary (for traditional medicine).
2. Has been coaching, training and was confirmed to have enough knowledge about the drug they were assigned referrer, the Pharmaceutical regulatory laws are concerned.
3. Do save for criminal liability and the Department of Health issued the card "the introduction of the drug".
Article 15: the powers, the responsibility of "the introduction": 1. information, advertising the drug to which they are assigned.
2. Only allowed introduction of smoking was allowed to circulate in Vietnam.
3. When you want to make the ad must present the card "the introduction" and the consent of the receiving place ads.
4. Collect the reports of side effects, harmful reactions, reports of drug quality defects and reflects the timeliness with which they represent: this unit is responsible for synthesizing and report to the Department of health, the Ministry of health (the Vietnam pharmaceutical Management Bureau).
Article 16. The case of the introduction of smoking would like to operate in a different local ads (not in the city, which introduced the drug card) must then be approved by the local health department where they plan promotional activities.
Article 17. "The introduction of the drug" is not used the physical benefits to cause emotional, convinced the medical officer in the prescription, drug consumption; not for sale or consignment of drugs.

Article 18. The medical facilities, hospitals, pharmacies, companies ... where people introduce drugs made the ads, is responsible for the review activities of the introduction of the drug; the case of the violation of the regulations must be reported immediately to the Department of health or the Ministry of health (the Vietnam pharmaceutical Management Bureau).
Article 19. Released promotional material is ad operations for medical officers by providing materials such as fact sheets, articles, magazine, map to introduce all materialize some items of a medicinal product as defined in article 10.
Article 20:1. Any promotional materials of a medicine for medical officers must also be limits, drafted according to the provisions of article 10 of this regulation.
2. the document cited, the document to illustrate retrieved from the magazine, reports science aims to elucidate the content says in article 10 to be honest, the Japanese pair and accompanied by a summary, the time of issuing the document.
3. Promotional materials are the Ministry of health; must record the license number, date of issue.
Article 21. Event promotional materials only invoice details one or some of the items specified in article 13, the rest must be in clear, not too little and to in the frame at the head or in the corner of the first page (see Appendix 4).
Article 22. The workshop introduced the drug: 1. Workshops to introduce the drug prescribed in this regulation is the drug product rollout or scientific seminars for medical cadres are related to smoking due to the production facilities, drug sponsors, business organization.
2. Only held workshops to introduce the drug was granted a registration number that allows circulating in Vietnam or were allowed to produce, circulate in other countries.
3. Content of the introduction of a drug product in the workshop must have the following (compare with drugs have the same effects are released).
Drug name: Miscellaneous Name (by the manufacturer).
Copyright international name (INN) or the original name (generic name).
Concentrations, the concentration of the active ingredient.
Dosage.
Pharmacokinetics.
Green pharmacy school.
Clinical information: specify.
Dosage, precautions note. Side effects, harmful reaction and how to handle.
Interactions between drugs.
Cases of overdose and handling.
Information on the patent: patent formulas.
Preserving, expires.
Packing.
Categorized under: poison, addictive drugs or special preservation area, the drug sold as single, selling is not needed.
Name, address of the manufacturer.
Article 23. Composition seminar introduced the drug must have at least 2/3 is the medical specialty, pharmacy staff. The report of the workshop is the professional officers, has extensive experience using the drug are being introduced.
Article 24:1. The drug production business unit would like to open a workshop to introduce the drug due to its production unit must obtain permission from the Ministry of health (the Vietnam pharmaceutical Management Bureau).
2. organizations, individual manufacturing, drug trading countries (stateless Vietnam) want to open a workshop to introduce the drug must have sufficient conditions: Must coordinate with 1 unit of Vietnam such as: medical clinic, Medical Academy, training medical personnel, production base business, medicine, pharmacology, Medical Society or other professional organizations. Are responsible for the activities in the course of the workshop.
Article 25. The conclusions, recommended in the workshop must be honest, consistent with the ideas discussed in the seminar and to report to the Ministry of health (Vietnam pharmaceutical Management Bureau) and can only be released after the permission of the Ministry of health (the Vietnam pharmaceutical Management Bureau).
Article 26. In the demo conferences, seminars of the medical officers: 1. The unit, the individual presiding over the Conference, seminar of medical officers like to organize the display, about smoking during the Conference, the Conference must get permission of the Ministry of health (the Vietnam pharmaceutical Management Bureau).
2. All activities of introduction of ad units have the drug exhibited during the Conference, the Conference must comply.
Article 27. Funding for conferences of medical officers: The production facilities, business funding allowed or material for the Conference of the medical staff but must ensure the following conditions: 1. The sponsor must be on a voluntary basis, without conditions attached and are publicly available.
2. The use of funding under the current rules.
 
CATEGORY B: DRUG ADS for the CHÚNGĐiều 28:1. Drug advertising activities for the public are conducted through the mass media such as radio, television, books, newspapers, brochures left ...
2. Possible images in advertising the drug to the public must be concise, general purpose, consistent with the level of understanding of the masses. Do not use the from exaggerated or words, images, sounds, triggers the following type of impression for the public: use this medication is the best measure, does not need the opinion of a physician.
This medicine completely harmless.
Article 29. A drug ad content to the public is presented in one of the following methods: method 1: contains the following information: the name of the drug: the name miscellaneous (by the manufacturer) the active ingredient or the original name (generic name).
Specify how to use contraindications things to avoid when using the name, the address of the manufacturing facility, to buy, to sell the drug.
Method 2: contains the following information: name of medication (as specified in method 1).
Specify the words said "read carefully the user manual before use".
Article 30. Prohibition of advertising the following drugs for the public: not yet granted Vietnam drug administration registration number, the registration number is expired or was revoked the registration number, the type out lets use.
The addictive drug, mental direction.
The single sold by pharmacies (prescription) of the physician.
The drugs specified in the following cases: tuberculosis sexually transmitted Diseases; aphrodisiac.
Heavy infections or bacterial infection spread.
Chronic insomnia.
Cancer, tumor diseases. Diabetes mellitus or other metabolic disorder diseases are similar.
Article 31. The amount of time the drug advertising to the public: a for advertising on daily newspapers (with categories for the medical industry) not extend beyond five days. A for advertising on television are not stretched too 8 days and not broadcast more than 5 times a day, on the radio not extend beyond 5 days and not broadcast more than 10 times a day. The waves separated by not less than 15 days.
An area of print advertising may not exceed 10% of the total area of the print press, advertising program duration may not exceed 5% of the broadcasting program.
Article 32. Drug advertising to the public on books, newspapers, magazines, brochures left: smoking aren't an advertising prohibition to the public stipulated in article 30, whether conditions are considering allowing the ads to the public through books, newspapers, magazines, brochures left.
Article 33. Drug ads on tv, broadcasting means: 1. The Ministry of Health announced the list of active substances to be reviewed, to allow advertising on tv, radio; This list is supplemented annually (annex 8).
2. The following conditions have to be reviews, allowing advertising on tv, radio.
Not in the smoking regulations in article 30.
No component active substances toxic under the current regulation.
There are obvious ingredients, easy to use.
Stable quality.
There is the main active ingredient is in the list of active substances to be reviewed, to allow advertising on tv, radio (see Appendix 8).
Article 34. Drug ads through the fair, the exhibition: 1. Only be exhibited in the fair, the exhibition has been issued the registration number to allow circulation. All the works on sale in fair, exhibitors must follow the current rules.

2. where the want on display, showcasing the product has not been granted registration number for travelling or other advertising activities must be The medical (pharmaceutical Management Department of Vietnam) review and permits.
Article 35. Drug ads on the other mass media: 1. Drug ads on the mass media is the advertising activities for the public on the mass media which are not specified in this regulation.
2. When the drug ads on the other mass media, to ensure that the current rules of the Ministry of culture and information and the other relevant regulations. 
 
CHAPTER II: AMERICAN ADVERTISING PHẨMĐiều 36. Cosmetic advertising provisions in this regulation is the active form of introducing public cosmetics on the mass media by the manufacturer, the cosmetics business implementation, funding to enhance the use, product consumption. Article 37. The cosmetics have enough following conditions are considering allowing ads: was the Ministry of health (the Vietnam pharmaceutical Management Bureau) arithmetic register allows the use, circulate in Vietnam.
Stable quality.
Article 38:1. The following products are not types of advertising: The type of cosmetics under the skin.
The cosmetics that use is likely to cause injury to the eyes, ears, nose, mouth mucosa.
The cosmetic use must have a physician's instructions.
2. Advertising Content cosmetics: Are objectivity, honestly, specifically, help for people using the correct, effective and safe.
The duration and the area under the right ad to the right provided for in article 31.
 
CHAPTER III: PROCEDURE for REQUESTING PERMISSION, BROWSE CONTENT and LICENSE the DRUG ADS, AMERICA PHẨMĐiều 39. Permission procedures, browse and tag "people introduce drugs". The Ministry of health authorize the Department of health, the card "the introduction of the drug". The individual units within and outside the country are practicing medicine in Vietnam send introduced drugs for his unit to do application allows local health department where the unit headquarters or representative office. Application for permission sent to "people introduce drugs" include: 1. Application for a permit (according annex 7).
2. the curriculum vitae of each person (certified local governments, home of the introduction of the drug).
3. Copy of diploma, doctor, pharmacist or health care salary (each person).
4. the health certificate (each person).
5. The list of items to be assigned referrer (each person).
6. Certificate of proficiency (each person) as defined in section 2, article 14.
Records made in 2 copies. After 30 days from the date of the application, the Department of health will answer litigants, case level must clearly indicate the reason. "People introduce drugs" worth 1 year from the date of issue; If you want to be given back "card people introduce drugs" unit shall submit the records before the expiration of 1 month.
The following case unit who introduced the drug must return the card "the introduction of drugs" for the Department of health: work unit change Only the task of introducing the drug expired.
Article 40: the Health Department must inspect organisation, confirmed the level of knowledge "who introduced the drug" as defined in section 2, article 14.
After 90 days from the date of this policy is in effect, the card "the introduction" has been issued ceases before the value.
Article 41:1 review, allowing print, released a document to ads for health officials: the unit has smoking been Vietnam Drug Administration issued the registration number allowing circulation like to print documents to advertise the drug for medical officers to send allows the Ministry of health (the Vietnam pharmaceutical Management Bureau); the records include: application (see annex 1).
The advertising content of each of the drugs specified in article 13 and annex 4.
Documents to verify the things stated in the advertising content of each drug.
Records made in 2 copies. Within a period of 60 days from the date of the application under the regulations, the Ministry of health (the Vietnam pharmaceutical Management Bureau) will answer litigants. The absence of consent must clearly indicate the reason.
2. Advertising materials most of the values in the following cases: drug items were withdrawn or eliminated from the index allows to use.
Change the information.
Individual units have the most valuable brochures are responsible for notification and recall.
Article 42. Review, allowing the workshop introduced, drug ads: the Ministry of health (the Vietnam pharmaceutical Management Bureau) review, licensing workshop introduction, drug ads; Records are: 1. Application for a permit (in annex 2).
2. Workshop program.
3. content of report, document presentation, intended for release in the workshop.
4. The document summary items advertised drugs.
5. Reference material.
Records made in 2 copies. After 30 days from the date of the application, the Ministry of health (the Vietnam pharmaceutical Management Bureau) will answer litigants. Cases not permit must clearly indicate the reason.
43 things. Review the content of drug advertising to the public on books, newspapers, magazines, brochures left.
The Ministry of health (the Vietnam pharmaceutical Management Bureau) and allowing drug ads to the public on books, newspapers, magazines, brochures left. The units have the drug granted the registration number that allows circulating in Vietnam want to advertise the drug on books, newspapers, magazines, the left must send the Ministry of health records (the Vietnam pharmaceutical Management Bureau). Records are: 1. Application for a permit (according to Appendix 1) 2. The advertising content (presented under article 29 and annex 3).
3. Document verifying the advertising content.
Records made in 2 copies. After 30 days from the date of the application rules the Ministry of health (Vietnam Drug Administration) will answer litigants. The absence of consent must clearly indicate the reason.
Article 44. Drug ads on tv, radio media: Ministry of health (the Vietnam pharmaceutical Management Bureau), license the drug ads on tv, the broadcasting media. The units have the drug granted the registration number that allows circulating in Vietnam want to drug ads on television, radio must send the Ministry of health records (the Vietnam pharmaceutical Management Bureau). Records are: 1. Application for a permit (according to Appendix 1).
2. Advertising content must be presented on paper and on tape. Lyrics, pictures, sound, music (if any) must conform to the provisions of section 2, article 28.
3. Document verifying the advertising content. Records made in 2 copies. After 30 days from the date of the application. The Ministry of health (the Vietnam pharmaceutical Management Bureau) will answer litigants. Cases not permit must clearly indicate the reason. The license has the value of 1 year from the date of signing. The case want to continue advertising should redo record, accompanied by statements made the previous ads license.
Article 45. Review for allowing drug ads during the fair, the exhibition: 1. The unit has joined the fair exhibition drugs must report the Ministry of health (the Vietnam pharmaceutical Management Bureau) and the local Health Department (which hosts the exhibition fair) on the program, the contents of his unit activities during the exhibition the fair, before 15 September.
2. Activities: workshops to introduce the drug, drug ads on the mass media of television, radio, print the document; must make application for permission (as specified in articles 41, 42, 43, 44).
Article 46. Review, allows cosmetic advertising: 1. The Ministry of health (the Vietnam pharmaceutical Management Bureau), allowing the advertising of cosmetics are the Ministry of Health issued the registration number to allow circulation. The unit wanted to do cosmetics ads send profile Vietnam drug administration. The records include: application (according to annex 6).
The advertising content.
Documents verifying the advertising content.
Records made in 2 copies. After 30 days from the date of receipt of sufficient profile Vietnam Drug Administration will reply to litigants. Cases not permit must clearly indicate the reason.

2. license allows the promotion of cosmetics worth 1 year from date of issue. The case want to continue advertising should redo the profile attached to the process report advertising license earlier.
 
CHAPTER IV: PROCESSING of MICRO-PHẠMĐiều 47. People who violate these rules, depending on the level of violation will be sanctioned administratively, to withdraw advertising, license record card "people introduce drugs", withdrawal of registration items of medicines, cosmetics or arrested save for criminal liability in accordance with the law. 
Chapter V: terms of CONTEST HÀNHĐiều 48. The unit in and out of the industry (including offshore units) is the practice of medicine, which had the drugs, cosmetics are the Ministry of Health issued the registration number for travelling in Vietnam, the units and individuals involved in information activities of drug ads, cosmetics on the territory of Vietnam is responsible for enforcement of this regulation. Article 49. Vietnam pharmaceutical Management Bureau, Department of health of the province, the central cities, health departments have the responsibility to guide the Organization, inspection, inspection of the implementation of "information regulation, advertising drugs and cosmetics for people".
ANNEX NO. 1 of the SOCIALIST REPUBLIC of VIETNAM established freedom NAMĐộc happy THUỐCKính AD APPLICATION: Drug Administration Viet Nam1. Unit name (individual) have been issued drug registration number: 2. Address: 3. The number of active licenses on firm level: 4. Please be advertising the following drugs: drug registration Number Name TT form the 5th ad. The documents include: the advertising content of each item of the document to verify the content of advertising copy license to operate industries 6. If the ad is licensed, we committed to fully implementing the existing regulations.
On September 1996 unit (individual) that the drug be given registration number APPENDIX No. 2 to the SOCIALIST REPUBLIC of VIETNAM independence freedom happiness SEMINAR APPLICATION SHOWCASE THUỐCKính sent: Drug Administration Viet Nam1. Unit name (or personal) Please open workshop: 2. Address: 3. Please open the Seminar introduced the drug: drug Name STT has been circulating in the country Of registration 4. Audience participation workshop: 5. Rapporteur: 6. the coordinating unit: 7. Hosts workshops: 8. seminar time: 9. The document must submit: the document will be used in workshops (under article 22; (3)) program workshop (expected).
The certificate of the product have been circulating.
On coordination unit in may 199 (stamp) unit Name (personal) Please open the workshop APPENDIX 3 PRESENTING ADVERTISING CONTENT for the PUBLIC: the FORM of SHEETS, books, BÁOGồm the following information: 1. The advertising content: includes lyrics and images, chart (if available).
2. License number, date of issue: 3. Sentence: "read carefully the user manual before use" eg: content advertising: Medinol Paracetamol 250 mg-containing solution, 0.5 ml in the case of: headache, migraine, toothache, sore throat, inflammation of the nerves.
Relief of symptoms: rheumatism, flu, fever due to a cold.
 
 
 
 
"Read carefully the user manual before use" No.:....................:...........
 
ANNEX No. 4: PRESENTING ADVERTISING CONTENT for medical OFFICERS LEAVE the SHEET FORMAT, books, BÁOGồm the following information: 1. The sentence: "the materials used for the medical staff." Ad content: includes lyrics and images, chart (if available) 3. Summary product information (see article 10) 4. License number, date of issue: for example, the materials used for the medical officer no. AD CONTENT:.................. Ngày.......................
APPENDIX 5: card who INTRODUCED the DRUG Including the following information: 1. Name the introduction of smoking (photo attached) 2. Address: 3. In the unit (company): address: 4. The powers, responsibilities (15; 17): 5. Card number: 6. Worth from: 7. The place and date of the card level: 8. Signed, stamped: APPENDIX 6CỘNG FREE SOCIALIST REPUBLIC NAMĐộc up happy freedom PETITION ADVERTISE cosmetics (cosmetics direct impact to human health) 1. Unit name (individual) there are cosmetic levels of registration: 2. Address: 3. The number of production licenses, business products, on level: 4. Pleased to advertise the following: cosmetics cosmetics Registration Number Name STT form the 5th ad. Please include the following documents: 5.1. Each ad content 5.2 cosmetics. Documents verifying the advertising content.
5.3. Copies of FDA manufacturing, cosmetics business.
6. If permitted we would commit to fully implementing the existing regulations related to advertising.
Hanoi, may day 199 units (individual) there are cosmetic levels of register APPENDIX 7 of the SOCIALIST REPUBLIC of VIETNAM established the happy freedom NAMĐộc APPLICATION SEND THUỐCKính send the INTRODUCTION: province Health Department (City) 1. Unit name people introduce drugs: 2. Address: 3. The number of active licenses of companies: 4. The elections (or contract) the following people go introduce smoking: S TT name year of birth professionalism Are the work (of residence) at 5. Training, training has been the work of drug introduction (stating the location, time, by one organization ...): 6. Please submit this form: by (or professional) in article 14; (1): test results about professional knowledge and pharmaceutical regulation by the Department of health:....................................................... Tổ chức ngày............................................
The Board assigned by the introduction of the drug unit.
On may 199 charge the unit NUMBER of the APPENDIX HAS the FOLLOWING MAJOR ACTIVE SUBSTANCES WILL BE REVIEWED, ALLOWING ADVERTISING to the PUBLIC on TELEVISION, radio, 1997 S TT active form of Name used to allow content of 1 Acefylin piperazin Member siro 500 mg Acetaminophen 500 mg uốngviên solution 2 3 DLLeucin injection form Minus the reductive acetyl-CoA 1, 5 g 4 skin Chrysophamic Acid 3% 5 LGlutamic Acid Tablets 500 mg 6 Acid 1 g 7 Tablets ascorbic Acid salicylic reductive acetyl-CoA Tablets 1 g boric Acid 8 drink powder in addition to citric Acid powdered drink Tablet 9 skin 2 g 10 200mg Park dimecrotic Acid salicylic Acid skin 11 12 tanic Acid using aqueous Tablet beyond undecylenic Acid skin 13 14 15 Albendazol Tablets 8 mg Tablets Acrivastine room hanging 400mg Alimemazine 16 drinking HCL oral solution 5 mg 16 Tablets Almagate aqueous Alpha tocopherol acetate 18 1 g oral liquid 400mg 19 Members
Aluminum hydroxid Staff Room 2 g oral suspension 20 amino acid acetic aqueous to drink 2 g 21 liquifae bactobacillus Member proteo & Amylo drink powder 150 mg 50 mg Tablet trithion Anethole 23 22 reductive acetyl-CoA Arginin asparaginate solution package nuggets drink 1 g external use fluids Argyrol 24 25 Viêndịch Astemizole Attapulgit 26 10 mg oral suspension oral 3 g Package Benzododecinium bromid solution used 27 out of 28 Bezoxonium chloride solution used beyond the 0, 1 g Tablet Berberin 29 30 powders online dedication
Member 3 g powder pack 31 Betain citra drinking fluids Members 32 33 Biocallular Bisacodyl 5 mg Tablets nuggets 34 Bromhexin hydrochloride oral solution 8 mg Tablets 35 mg of caffeine Tablets 0, 05g 36 alphaacetoglutarat 37 Viênsiro tube Calcibromogalactogluconat 2 g Calcium drink 5 g 38 Calcicarbonat 39 Calcigluconat 5 g powder Pack Pellets pellets 5 g 40 Calciphospghat 41 2 g Camphor powder package User Members in addition to High liver 42 Staff Members Carbinoxamin 43 drinking fluids to drink fluids 44 solution 4 mg Tablet Carbocystein drink 0, 5 g 45 Cethexonium 46 Cetomacrogol external Users also Use bromure 47 Chlorpheniramin Tablets 4 mg oral solution 48 Chondroitin Tablet oral solution 10 g 49 sulphat Cimetidin Tablets 25 mg Capsule Cinnarinine 800mg 50 51 52 Clorhexidine external Users also Use Cloramphenicol 53 Clotrimazon 54 Cod liver oil also Used Staff liquid drink 55 Creosete 56 oral Use Crotamiton solution Members in addition to the drinking tube Cyanocobalatin 57 D 58 59 5 mg Tablet pharmacy paraffin Oil Biotin application solution drink used in addition to 60 Diqualinium ngậmkem BOI 0, 5 mg Tablets chlorite 61 62 Diethylamin misting Member Dexpanthenol salicylate Use outside Diethylamin salicilat 63 64 65 100 mg Tablet Dimenhydrynat also Uses Dimethycone Viêncốmdịch hang Dimethyldene 66

Oral solution 5 mg, 2 capsules 67 Diosmin 68 succinat Doxylamin 500 mg powder package Staff Members also Use Econazol 69 15 mg syrup Etamsylat 500 mg Tablets 70 71 72 Ferrous fumarate Tablets Eucalipol User external oral solution Ferrous sulfate Tablets 73 74 200mg 200mg Guaiazulen User external Sulfaguanidin 75 Members 0, 5 g Glucose drink Viênbột 76 77 78 oral solution of Glycerin Hemoglobin Siro aqueous drink Ibuprofen oral suspension néndịch Park 79 400 mg 80 Iodotanic Siro 81 Isothipendyn HCL
Staff Use beyond 12 mg 82 K Gluconate Tablets oral solution 1 g Potassium chloride Tablets 1 g powder pack 83 84 85 Keroconazol User external User sulfate Zinc also 86 KMnO4 (purple pills) is used in addition to drinking fluids isoleucin, L 87 88 Lactobacillus acidophilus oral tube 89 acetylsalicylate Lysine tablets Pack Package 1 g Magnesium sulfate 30 g Pack of 90 91 92 Mannitol Magnesium hydroxid Staff hanging 1520g drink Powder Room 93 Mebendazol Members 94 lauryle Mercryl 500 mg solution Used in addition
 
95 ngậmDùng 96 Mequitazin Park outside Officer Menthol 5 mg Tablets 5 mg Methionine 97 98 99 external Use Sodium Methyl salicylate hydrocarbonat Pack of 100 pellets sodium benzoate Tablets oral solution Sodium thiosulfat 101 102 Oxeladin Citrate 2 g Member Member Member Oxerutin 104 103 Oxygen 60mg Siro elderly User out 105 106 107 Member Phenolphtalein external User Oxytetracyclin Phytomennadion 108 10 mg Tablet Pidolat calcium drinking tube 109 Piperazine Member 3 g 110 HCL Staff Promethazin siro siro 50 mg Pyrantel pamoat 111
Staff room hanging tube 112 500 mg Pyridoxine HCL Tablets Piroxicam Use outside 113 114 115 300mg Tablets 250 mg Retinol Member Concierge Ranitidin hanging 50,000 unit 116 117 118 Bộtcốmviên Saccharomyces 10 mg Tablets of Riboflavin Tetrahydrozoline Used in addition to 119 120 Tioconazol User external 250 mg Tablets Thiamine 121 122 Tribenoside Staff also Use oxyd Titanium Used in addition to 400mg 123 Viênsiro 2 Triprolidin 124 external User Triclocarban, 5 mg Tablet metylen Blue AQ 125 126 The ethnic medicine (drug review each the specific case) maximum compounds allowed in drug form