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
Kanka Triple Action BENZOCAINE and MENTHOL, UNSPECIFIED FORM BENZOCAINE BENZOCAINE MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM POLYETHYLENE GLYCOL, UNSPECIFIED POLYETHYLENE GLYCOL 3350 SUCRALOSE PHENOXYETHANOL ASCORBYL PALMITATE THYMOL CETYLPYRIDINIUM CHLORIDE
spl unclassified section
Drug Facts
活性成分 / Active ingredient
Active ingredients Purpose Benzocaine 20.0% (w/w) Oral anesthetic/analgesic (oral pain reliever) Menthol 2.0% (w/w) Oral anesthetic/analgesic (oral pain reliever)
active ingredient table
<table width="60%"><col width="40%" align="left" valign="top"/><col width="60%" align="right" valign="top"/><thead><tr><th><content styleCode="italics">Active ingredients</content></th><th><content styleCode="italics">Purpose</content></th></tr></thead><tbody><tr><td>Benzocaine 20.0% (w/w)</td><td>Oral anesthetic/analgesic (oral pain reliever)</td></tr><tr><td>Menthol 2.0% (w/w)</td><td>Oral anesthetic/analgesic (oral pain reliever)</td></tr></tbody></table>
用途 / Purpose
Active ingredients Purpose Benzocaine 20.0% (w/w) Oral anesthetic/analgesic (oral pain reliever) Menthol 2.0% (w/w) Oral anesthetic/analgesic (oral pain reliever)
purpose table
<table width="60%"><col width="40%" align="left" valign="top"/><col width="60%" align="right" valign="top"/><thead><tr><th><content styleCode="italics">Active ingredients</content></th><th><content styleCode="italics">Purpose</content></th></tr></thead><tbody><tr><td>Benzocaine 20.0% (w/w)</td><td>Oral anesthetic/analgesic (oral pain reliever)</td></tr><tr><td>Menthol 2.0% (w/w)</td><td>Oral anesthetic/analgesic (oral pain reliever)</td></tr></tbody></table>
适应证 / Indications and usage
Uses for the temporary relief of pain associated with canker sores, minor irritation of the mouth and gums caused by dentures or orthodontic appliances, or minor injury of the mouth or gums.
警告 / Warnings
Warnings METHEMOGLOBINEMIA WARNING Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: pale, gray, or blue colored skin (cyanosis) headache rapid heart rate shortness of breath dizziness or lightheadedness fatigue or lack of energy Allergy alert do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics. Do not use for teething in children under 2 years of age When using this product do not use this product for more than 7 days unless directed by a dentist or doctor. If sore mouth symptoms do not improve in 7 days; if irritation, pain, or redness persists or worsens; or if swelling, rash or fever develops, see your dentist or doctor promptly. do not exceed recommended dosage. Keep out of reach of children. If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away.
禁用事项 / Do not use
Do not use for teething in children under 2 years of age
使用中 / When using
When using this product do not use this product for more than 7 days unless directed by a dentist or doctor. If sore mouth symptoms do not improve in 7 days; if irritation, pain, or redness persists or worsens; or if swelling, rash or fever develops, see your dentist or doctor promptly. do not exceed recommended dosage.
儿童安全 / Keep out of reach of children
Keep out of reach of children. If more than used for pain is accidentally 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 Apply to affected area up to 4 times daily or as directed by a dentist or doctor Children between 2 and 12 years of age Ask a doctor before use. Should be supervised in the use of this product Children under 2 years of age Do not use
dosage and administration table
<table width="60%"><col width="50%" align="left" valign="top"/><col width="50%" align="left" valign="top"/><tbody><tr styleCode="Botrule"><td styleCode="Rrule">Adults and children 2 years of age and older</td><td>Apply to affected area up to 4 times daily or as directed by a dentist or doctor</td></tr><tr styleCode="Botrule"><td styleCode="Rrule">Children between 2 and 12 years of age</td><td>Ask a doctor before use. Should be supervised in the use of this product</td></tr><tr styleCode="Botrule"><td styleCode="Rrule">Children under 2 years of age</td><td>Do not use</td></tr></tbody></table>
储存 / Storage and handling
Other information www.kank-a.com
辅料 / Inactive ingredients
Inactive ingredients ascorbyl palmitate, cetylpyridinium chloride, PEG-75, phenoxyethanol, polyethylene glycol, sucralose, thymol
package label principal display panel
PRINCIPAL DISPLAY PANEL - 11.9 g Tube Carton MAXIMUM STRENGTH KANKA ® TRIPLE ACTION GEL ORAL PAIN RELIEVER Mouth Pain Relief for Canker Sores Net Wt. 0.42 oz. (11.9 g) Principal Display Panel - 11.9 g Tube Carton
来源、版本与许可
- 资料类型
- 美国药品标签原文
- 版本
- 1 / 20250109
- 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.

