View Drug - Kanka Triple Action
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Kanka Triple Action

Generic: BENZOCAINE AND MENTHOL, UNSPECIFIED FORM

100%
Basic Information
Manufacturer
Blistex Inc.
Product Type
HUMAN OTC DRUG
Route of Administration
ORAL
FDA Set ID
078fcdab-38a1-4a9a-bdd3-e17446591ea8
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)
Indications & 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.
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.