ZenTrip Motion Sickness
ZenTrip Motion Sickness is an FDA drug label for the active ingredient MECLIZINE HYDROCHLORIDE manufactured by Sato Pharmaceutical Co., LTD administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231103.
Generic: MECLIZINE HYDROCHLORIDE
Manufacturer: Sato Pharmaceutical Co., LTD
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 49873-805
Application: M009
Effective: 20231103
Active Ingredients: Active ingredient (in each tablet) Meclizine hydrochloride 25mg
Indications & Usage
Uses for the prevention and treatment of the nausea, vomiting, or dizziness associated with motion sickness
Dosage & Administration
Directions to prevent motion sickness, take it at least one hour before traveling adults and children 12 years of age and over: take 1 to 2 tablets (25 to 50mg) once daily, or as directed by a physician.
Contraindications
Not available.
Warnings
Warnings Do not use in children under 12 years of age unless directed by a physician Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis difficulty in urination due to enlargement of the prostate gland Ask a physician or pharmacist before use if you are taking sedatives or tranquilizers When using this product you may get drowsy be careful when driving a motor vehicle or operating machinery alcohol, sedatives, and tranquilizers may increase the drowsiness effect avoid alcoholic beverages If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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