说明与适用边界
此页按所列地区、版本归档。标签内容可能更新,具体产品请核对原始来源;本站关联表示阅读线索,不表示药品与器械可兼容或可替换。
spl product data elements
Nuvicare-Allergy Relief Loratadine Tablets, 10 mg loratadine LORATADINE LORATADINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE povidone STARCH, CORN P;10
spl unclassified section
Drug Facts
活性成分 / Active ingredient
Active Ingredient (in each tablet) Loratadine, 10 mg
用途 / Purpose
Purpose Antihistamine
适应证 / Indications and usage
Uses Temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
警告 / Warnings
Warnings Do not use if you ever have had an allergic reaction to this product or any of its ingredients.
咨询医生 / Ask a doctor
Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
使用中 / When using
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
停用事项 / Stop use
Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
孕哺期 / Pregnancy or breastfeeding
If pregnanct or breast-feeding , ask a health professional before use.
儿童安全 / Keep out of reach of children
Keep out of reach of children . In case of overdose, get medical help or contact a poison control center right away (1-800-222-1222)
用法用量原文 / Dosage and administration
Directions Adults and children 6 years and over: 1 tablet daily; not more than 1 tablet in 24 hours. Children under 6 years of age: Ask a doctor. Consumers with liver or kidney disease: Ask a doctor
其他安全资料 / Other safety information
Other Information Store between 20° to 25°C (68° to 77°F) (see USP Controlled Room Temperature) Protect from excessive moisture
辅料 / Inactive ingredients
Inactive ingredients Lactose monohydrate, magnesium stearate, povidone, maize starch, purified water.
questions
Questions or comments? Call 1(718) 337-8733 or email: [email protected]
package label principal display panel
PL0270-00 NC Allergy Relief-Loratadine 100ct
来源、版本与许可
- 资料类型
- 美国药品标签原文
- 版本
- 1 / 20250701
- 获取时间
- 2026-10-08
- 许可
- openFDA public data; retain original label attribution. See 查看来源 and dataset source notices. Public access does not imply approval or unrestricted rights to every submitted label.

