说明与适用边界
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spl product data elements
Cetirizine Hydrochloride Cetirizine Hydrochloride Allergy CETIRIZINE HYDROCHLORIDE CETIRIZINE SILICON DIOXIDE CROSCARMELLOSE SODIUM HYPROMELLOSE 2910 (5 MPA.S) LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 400 TITANIUM DIOXIDE White to Off-white X;36
spl unclassified section
Drug Facts
活性成分 / Active ingredient
Active ingredient (in each tablet) Cetirizine hydrochloride USP 10 mg
用途 / Purpose
Purpose Antihistamine
适应证 / Indications and usage
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
警告 / Warnings
Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.
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.
咨询医药人员 / Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.
使用中 / When using
When using this product drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery
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 pregnant or breast-feeding: If breast-feeding: not recommended if pregnant: 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 one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. adults 65 years and over ask a doctor children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor
dosage and administration table
<table cellspacing="0" cellpadding="0" border="0" width="776.72"><colgroup><col width="45.3767123287671%"/><col width="54.6232876712329%"/></colgroup><tbody><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top">adults and children 6 years and over </td><td styleCode="Rrule" valign="top">one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top">adults 65 years and over </td><td styleCode="Rrule" valign="top">ask a doctor </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top">children under 6 years of age </td><td styleCode="Rrule" valign="top">ask a doctor </td></tr><tr><td styleCode="Lrule Rrule" valign="top">consumers with liver or kidney disease </td><td styleCode="Rrule" valign="top">ask a doctor </td></tr></tbody></table>
储存 / Storage and handling
Other information store between 20° to 25°C (68° to 77°F) TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING.
辅料 / Inactive ingredients
Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.
questions
Questions? call 1-855-274-4122 DISTRIBUTED BY CARDINAL HEALTH DUBLIN, OHIO 43017 www.myleader.com 1-800-200-6313 Made in India Code: TS/DRUGS/19/1993
package label principal display panel
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (365's Tablets Bottle) LEADER TM NDC 70000-0047-1 Original Prescription Strength All Day Allergy Cetirizine Hydrochloride Tablets USP, 10 mg | Antihistamine COMPARE TO ZYRTEC ® active ingredient * Indoor and Outdoor Allergies 24-Hour Relief of: Sneezing; Runny Nose; Itchy, Watery Eyes; Itchy Throat or Nose 365 TABLETS 10 mg EACH PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (14's Tablet Blister Pack Label)
来源、版本与许可
- 资料类型
- 美国药品标签原文
- 版本
- 4 / 20251003
- 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.

