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西药 · 美国药品标签原文

HISTEX PD Drops New Formulation

TRIPROLIDINE HYDROCHLORIDE

HISTEX PD Drops New Formulation · Allegis Pharmaceuticals, LLC。此记录对应特定产品,标签收录不代表所有用途获批。

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

HISTEX PD Drops New Formulation TRIPROLIDINE HYDROCHLORIDE SUCRALOSE SODIUM BENZOATE CITRIC ACID MONOHYDRATE GLYCERIN PROPYLENE GLYCOL WATER SODIUM CITRATE, UNSPECIFIED FORM SORBITOL TRIPROLIDINE HYDROCHLORIDE TRIPROLIDINE

spl unclassified section

Drug Facts

活性成分 / Active ingredient

Active ingredient (in each 1 mL dropperful) Triprolidine HCl 1.25 mg

用途 / Purpose

Purpose Antihistamine

适应证 / Indications and usage

Uses temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes

警告 / Warnings

Warnings Do not exceed recommended dosage. Ask a doctor before use if the child has a breathing problem such as emphysema or chronic bronchitis glaucoma Ask a doctor before use if the child is taking sedatives or tranquilizers When using this product excitability may occur, especially in children may cause drowsiness sedatives and tranquilizers may increase the drowsiness effect Stop use and ask a doctor if new symptoms occur Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

禁用事项 / Do not use

Do not exceed recommended dosage.

咨询医生 / Ask a doctor

Ask a doctor before use if the child has a breathing problem such as emphysema or chronic bronchitis glaucoma

咨询医药人员 / Ask a doctor or pharmacist

Ask a doctor before use if the child is taking sedatives or tranquilizers

使用中 / When using

When using this product excitability may occur, especially in children may cause drowsiness sedatives and tranquilizers may increase the drowsiness effect

停用事项 / Stop use

Stop use and ask a doctor if new symptoms occur

儿童安全 / Keep out of reach of children

Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

用法用量原文 / Dosage and administration

Directions Do not exceed recommended dosage. use only the enclosed dropper. do not use enclosed dropper for any other drug products. AGE DOSE Adutls & Children 12 years of age or older: 2 mL (2.5 mg) every 4 to 6 hours, not to exceed 8 mL (10 mg) in 24 hours or as directed by a doctor. Children 6 to under12 years of age: 1 mL (1.25 mg) every 4 to 6 hours, not to exceed 4 mL (5 mg) in 24 hours or as directed by a doctor. Children under 6 years of age: Consult a docotor.

dosage and administration table

<table width="75%"><colgroup><col align="left" valign="top" width="40%"/><col align="left" valign="top" width="60%"/></colgroup><thead><tr><th styleCode="Rrule">AGE</th><th>DOSE</th></tr></thead><tbody><tr styleCode="Botrule"><td styleCode="Rrule">Adutls &amp; Children 12 years of age or older:</td><td>2 mL (2.5 mg) every 4 to 6 hours, not to exceed 8 mL (10 mg) in 24 hours or as directed by a doctor.</td></tr><tr styleCode="Botrule"><td styleCode="Rrule">Children 6 to under12 years of age:</td><td>1 mL (1.25 mg) every 4 to 6 hours, not to exceed 4 mL (5 mg) in 24 hours or as directed by a doctor.</td></tr><tr><td styleCode="Rrule">Children under 6 years of age:</td><td>Consult a docotor.</td></tr></tbody></table>

储存 / Storage and handling

Other Information Store at 15°-30° C (59°-86° F). Tamper evident by foil seal under cap. Do not use if foil seal is missing or broken.

辅料 / Inactive ingredients

Inactive ingredients bubble gum flavor, citric acid, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose.

questions

Questions? Comments? Call 1-866-633-9033.

package label principal display panel

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton NDC 28595-809-30 HISTEX™ PD New Formulation Drops Antihistamine Each dropperful (1 mL) contains: Triprolidine HCl 1.25 mg Sugar-Free • Dye Free Alcohol Free Bubble Gum Flavor 1 fl oz (30 mL) Bottle Label

来源、版本与许可

资料类型
美国药品标签原文
版本
3 / 20250108
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.
核对原始来源