Fufang Zijing Pishui Yangsuan Rongye (复方紫荆皮水杨酸溶液)复方紫荆皮水杨酸溶液
This is a medicine registration record from NMPA data.本页为国家药监局药品注册记录。
Labeled sections from the recorded Chinese source are included below. English wording is a reference translation when one is on file, not an official English label.本记录未接入产品级适应症/安全性标注字段。
生产企业Manufacturer
- 江西普丽尔药业有限公司Chinese legal name: 江西普丽尔药业有限公司
主要成分Active Ingredients
- 苯甲酸Benjia Suan
- 毫克Hao Ke
- 紫荆皮毫克Zijing Pihao Ke
- 冰醋酸毫克Bingcu Suanhao Ke
- 苯海拉明毫克Benhai Laming Haoke
- 辅料为Excipients recorded as
药物知识说明
苯甲酸是一种在国家药监局注册认定的药品。该药品含有相关活性成分。
该药品关联的活性成分包括：毫克、苯海拉明毫克、苯甲酸Benjia Suan。这些成分信息来自国家药监局数据库。
您可以探索含有相同成分的其他药品：毫克-1be7a837成分药品。
本页面内容来自国家药监局数据库，MedicineGraph在此基础上提供关系图谱和知识导航。
Medicine Knowledge
This medicine (original name: 复方紫荆皮水杨酸溶液) is a medicine registered with the national drug regulatory authority. It contains active ingredient(s) as recorded.
Active ingredients associated with this product: 苯甲酸Benjia Suan.
Explore other medicines containing the same ingredient: 毫克 productsProducts containing this recorded ingredient.
Source: MedicineGraph authoritative database. Relationships derived from registered product information.
这是什么What is this
- 通用名/品名Recorded product name: 复方紫荆皮水杨酸溶液Recorded Chinese name: 复方紫荆皮水杨酸溶液
- 剂型Dosage form: 溶液剂Solution
- 规格Specification: 复方Recorded Chinese specification
本段仅展示注册/说明书已记录的身份属性，不含适应症或用法建议。Identity attributes from registration/leaflet records only; no indications or usage advice.
主要成分Ingredients
生产企业Manufacturer
- 江西普丽尔药业有限公司Chinese legal name: 江西普丽尔药业有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字H20083553
关联实体Relationships
信息来源Source and scope
国家药品监督管理局（中国）药品注册数据及已接入说明书字段。National Medical Products Administration (China) medicine-registration data and linked leaflet fields.
- 品名来源Name source: 10多万条药品说明书数据库 (HIGH)Package-insert database (more than 100,000 records) (HIGH)
- 生产企业来源Manufacturer source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
- 剂型来源Dosage-form source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
范围：当前 MedicineGraph 注册记录及已记录的精确关系；非完整目录，亦不构成疗效等同主张，也不支持换用判断。不含适应症/安全性推断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence. No inferred indications/safety.
本段为已核准说明书原文摘录（非改写、非AI摘要），非正式英文标签，亦不构成用药建议。 Not an official English label and not medical advice. English wording, when shown, is a reference translation of the Chinese source label.
English translation for reference. Translated from the Chinese source label. Not an official English label and not medical advice.
NMPA approval number
国药准字H20083553
Manufacturer
Chinese legal name: 江西普丽尔药业有限公司 (domestically manufactured)
Indications
English translation unavailable. The original Chinese source label remains available below.
Dosage and administration
English translation unavailable. The original Chinese source label remains available below.
Adverse reactions
English translation unavailable. The original Chinese source label remains available below.
Contraindications
English translation unavailable. The original Chinese source label remains available below.
Precautions
English translation unavailable. The original Chinese source label remains available below.
Storage
English translation unavailable. The original Chinese source label remains available below.
Specification
English translation unavailable. The original Chinese source label remains available below.
中文说明书原文Original Chinese source label
批准文号
国药准字H20083553
生产企业
江西普丽尔药业有限公司(国产)
适应症
用于足癣，亦用于手足多汗症。
用法用量
外用，涂患处，每3日一次
不良反应
偶见皮肤刺激如烧灼感，或过敏反应如皮疹、瘙痒等。
禁忌
患处已皲裂、糜烂或感染者禁用。
注意事项
1.避免接触眼睛和其他黏膜（如口、鼻等）。
2.用药部位如有烧灼感、红肿等情况应停药，并将局部药物洗净，必要时向医师咨询。
3.本品为外用制剂，切勿口服，并避免大面积使用。
4.肾功能不全者、孕妇以及哺乳期妇女慎用。
5.对本品过敏者禁用，过敏体质者慎用。
6.本品性状发生改变时禁止使用。
7.请将本品放在儿童不能接触的地方。
8.儿童必须在成人监护下使用。
9.如正在使用其他药品，使用本品前请咨询医师或药师。
贮藏
遮光，密闭，阴凉干燥处保存。
规格
复方
信息来源Source and scope
国家药品监督管理局（中国）药品注册数据。National Medical Products Administration (China) medicine-registration data.
范围：当前 MedicineGraph 注册记录及已记录的精确关系；非完整目录，亦不构成疗效等同主张，也不支持换用判断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence.