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西药 · 美国药品标签原文

Target Up and Up Pain Relieving Cleansing

BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE

Target Up and Up Pain Relieving Cleansing · TARGET CORPORATION。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

Target Up and Up Pain Relieving Cleansing Benzalkonium Chloride and Lidocaine Hydrochloride WATER BENZALKONIUM CHLORIDE BENZALKONIUM LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS SODIUM HYDROXIDE EDETATE DISODIUM ALCOHOL PROPYLENE GLYCOL

活性成分 / Active ingredient

Active Ingredients Benzalkonium Cl 0.13% Lidocaine HCL 2.5%

用途 / Purpose

Purpose First aid antiseptic Pain relieving spray

适应证 / Indications and usage

Uses first aid to help prevent bacterial contamination or skin infection and for temporary relief of pain and itching associated with minor: cuts scrapes minor burns sunburn minor skin irritations

警告 / Warnings

Warnings For external use only

咨询医生 / Ask a doctor

Ask a doctor before use if you have deep or puncture wounds animal bites serious burns

使用中 / When using

When using this product do not use in or near the eyes do not apply over large areas of the body or in large quantities do not apply over raw surfaces or blistered areas

停用事项 / Stop use

Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days, or clear up and occur again within a few days

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 and older: clean the affected area; apply a small amount on the area 1-3 times daily may be covered with a sterile bandage if bandaged, llet dry first children under 2 years, ask a doctor

储存 / Storage and handling

Other information avoid excessive heat store at room temperature

辅料 / Inactive ingredients

Inactive ingredients alcohol, disodium EDTA, fragrance, propylene glycol, purified water, sodium hydroxide

package label principal display panel

Label 82938EF

来源、版本与许可

资料类型
美国药品标签原文
版本
2 / 20240125
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