Xiaoer Qingre Ling (小儿清热灵)小儿清热灵
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
- 长春银诺克药业有限公司Chinese legal name: 长春银诺克药业有限公司
主要成分Active Ingredients
- 普拉睾酮Pula Gaotong
药物知识说明
普拉睾酮是一种在国家药监局注册认定的药品。该药品含有普拉睾酮-74e78cd6等成分。
该药品关联的活性成分包括：普拉睾酮Pula Gaotong。这些成分信息来自国家药监局数据库。
该药品标注的生产企业为：长春银诺克药业有限公司Chinese legal name: 长春银诺克药业有限公司。
您可以探索含有相同成分的其他药品：普拉睾酮-74e78cd6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: 小儿清热灵) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).
Active ingredients associated with this product: 普拉睾酮Pula Gaotong.
Manufacturers recorded for this product: 长春银诺克药业有限公司Chinese legal name: 长春银诺克药业有限公司.
Explore other medicines containing the same ingredient: 普拉睾酮 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: 小儿清热灵Recorded Chinese name: 小儿清热灵
- 规格Specification: 每片0.1gRecorded 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
- 长春银诺克药业有限公司Chinese legal name: 长春银诺克药业有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字Z22020329
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)
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Z22020329
Manufacturer
Chinese legal name: 长春银诺克药业有限公司 (domestically manufactured)
Traditional functions
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Z22020329
生产企业
长春银诺克药业有限公司(国产)
功能主治
1.本品用于清热解毒,利咽止咳。 2.本品用于感冒发热,咽喉肿痛,咳嗽气喘。
用法用量
口服,一日2次。 1.6个月以下小儿一次1/2片; 2.7～10个月一次1片; 3.1～2岁一次1.5片； 4.2～3岁一次2片; 5.3岁以上3～5片;
不良反应
尚不明确。
禁忌
对本品过敏者禁用。
注意事项
1.忌食辛辣、生冷、油腻食物。
2.风寒感冒者不适用,表现为发热畏冷、肢凉、流清涕,咽不红者。
3.婴幼儿及糖尿病患儿应在医师指导下应用。
4.脾虚易腹泻者慎服。
5.严格按照用法用量服用,服药3天症状无缓解,应去医院就诊。本品不宜长期服用。
6.对本品过敏者禁用,过敏体质者慎用。
7.本品性状发生改变时禁止使用。
8.儿童必须在成人监护下使用。
9.请将本品放在儿童不能接触的地方。
10.如正在使用其他药品,使用本品前请咨询医师或药师。
贮藏
密封，在干燥处保存。
规格
每片0.1g
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.