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西药 · 美国药品标签原文

利多卡因 · LidoPlus Pain Relief

LIDOCAINE HYDROCHLORIDE

LidoPlus Pain Relief · Centura Pharmaceuticals, Inc。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

LidoPlus Pain Relief LIDOCAINE HYDROCHLORIDE ALOE VERA LEAF WATER ARNICA MONTANA FLOWER INDIAN FRANKINCENSE C13-14 ISOPARAFFIN CETYL ALCOHOL ETHYLHEXYLGLYCERIN GLUCOSAMINE SULFATE GLYCERYL MONOSTEARATE GLYCERIN HAMAMELIS VIRGINIANA TOP LAURETH-7 PEG-100 STEARATE PHENOXYETHANOL POLYSORBATE 20 STEARIC ACID LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE

spl unclassified section

Drug Facts

活性成分 / Active ingredient

Active Ingredients: Lidocaine HCl 4.00% Topical Anesthetic

用途 / Purpose

Topical Anesthetic

适应证 / Indications and usage

Indications: For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites and minor skin irritations.

警告 / Warnings

Warnings: For external use only. • Avoid contact with eyes. • If condition worsens or symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not use in large quantities, particularly over raw surfaces or blistered areas. If pregnant or breast feeding, contact physician prior to use.

儿童安全 / Keep out of reach of children

Keep out of reach of children. If swallowed, consult physician.

禁用事项 / Do not use

Do not use in large quantities, particularly over raw surfaces or blistered areas.

孕哺期 / Pregnancy or breastfeeding

If pregnant or breast feeding, contact physician prior to use.

用法用量原文 / Dosage and administration

Directions: • Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. • Children under two-years of age: consult a physician.

辅料 / Inactive ingredients

Other Ingredients: Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, C13-14 Isoparaffin, Cetyl Alcohol, Chondroitin Sulfate, Dimethyl Sulfone (MSM), Ethylhexylglycerin, Glucosamine Sulfate, Glyceryl Stearate, Glycerin, Hamamelis Virginiana (Witch Hazel) Extract, Laureth-7, PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate-20, Stearic Acid.

package label principal display panel

Package Labeling: Label 2

来源、版本与许可

资料类型
美国药品标签原文
版本
7 / 20260112
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