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西药 · 美国药品标签原文

Olopatadine Hydrochloride Ophthalmic Solution

OLOPATADINE HYDROCHLORIDE OPHTHALMIC

Olopatadine Hydrochloride Ophthalmic Solution · Walgreens Company。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

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spl product data elements

Olopatadine Hydrochloride Ophthalmic Solution Olopatadine Hydrochloride Ophthalmic OLOPATADINE HYDROCHLORIDE OLOPATADINE BENZALKONIUM CHLORIDE SODIUM PHOSPHATE, DIBASIC HYDROCHLORIC ACID SODIUM CHLORIDE SODIUM HYDROXIDE WATER carton Label

活性成分 / Active ingredient

ACTIVE INGREDIENT Olopatadine (0.1%) (equivalent to olopatadine hydrochloride 0.111%)

用途 / Purpose

PURPOSE Antihistamine and redness reliever

适应证 / Indications and usage

USES temporarily relieves itchy and red eyes due to pollen, ragweed, grass, animal hair and dander

警告 / Warnings

WARNINGS For external use only

禁用事项 / Do not use

DO NOT USE • if solution changes color or becomes cloudy • if you are sensitive to any ingredient in this product • to treat contact lens related irritation

使用中 / When using

WHEN USING THIS PRODUCT do not touch tip of container to any surface to avoid contamination remove contact lenses before use wait at least 10 minutes before reinserting contact lenses after use do not wear a contact lens if your eye is red

停用事项 / Stop use

STOP USE AND ASK DOCTOR IF you experience: eye pain changes in vision increased redness of the eye itching worsens or lasts for more than 72 hours

儿童安全 / Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a Poison Control Center right away.

用法用量原文 / Dosage and administration

DIRECTIONS • adults and children 2 years of age and older: • put 1 drop in the affected eye(s) twice daily, every 6 to 8 hours, no more than twice per day • if using other ophthalmic products while using this product, wait at least 5 minutes between each product • replace cap after each use • children under 2 years of age: consult a doctor

其他安全资料 / Other safety information

OTHER INFORMATION • only for use in the eye • store between 4° to 25°C (39° to 77°F)

辅料 / Inactive ingredients

INACTIVE INGREDIENTS Benzalkonium chloride 0.01%, Dibasic sodium phosphate, Hydrochloric acid and /or Sodium hydroxide (to adjust pH), Sodium chloride and Water for Injection.

questions

QUESTIONS? Call 1-888-375-3784

package label principal display panel

PRINCIPAL DISPLAY PANEL NDC 0363-7130-05

来源、版本与许可

资料类型
美国药品标签原文
版本
4 / 20251210
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