MedDataToolMedDataTool

Bonine Max

Generic: Meclizine Hydrochloride

OTC
Antiemetic✓ FDA-verified
View full FDA label ↗
Bonine Max is a medication that helps prevent and treat nausea, vomiting, or dizziness caused by motion sickness. It works by calming the signals in the brain that trigger these symptoms. You should take one chewable tablet once a day, ideally one hour before you travel, and make sure to chew or crush it completely before swallowing. It's important to note that this medication should not be used by children under 12 unless directed by a doctor. Additionally, if you are taking sedatives or tranquilizers, you should ask your doctor or pharmacist before using it, as these can increase drowsiness.

Uses

  • nausea. vomiting. dizziness associated with motion sickness.

Dosage

Take 1 chewable tablet one hour before travel.
Do not take more than directed.
Adults and children 12 years and older: take 1 tablet once daily or as directed by a doctor.
Chew or crush the tablet completely before swallowing; do not swallow whole.
Always follow your doctor's specific instructions for your dose.

Side effects

Common

Drowsiness may occurSeek medical help for overdose
🛑

Warnings

⚠ Important warnings

  • Do not use for children under 12 unless directed by a doctor.
  • Ask a doctor before use if you have difficulty urinating, glaucoma, or breathing problems.
  • Alcohol, sedatives, and tranquilizers may increase drowsiness.
  • Use caution when driving or operating machinery.
  • If pregnant or breastfeeding, ask a health professional before use.

Drug interactions

  • Sedativesmay increase drowsinessCaution
  • Tranquilizersmay increase drowsiness.Caution

Ask about this product

Answers pulled from the FDA label only.

AI
Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).