Home > Drugs A-Z > Zentrip

Zentrip (Sato Pharmaceutical Co., Ltd.)

Available Formats

Dosage Form Package Information Links
FILM, SOLUBLE 8 PACKET in 1 CARTON (49873-803-01) > 1 FILM, SOLUBLE in 1 PACKET Label Information

Complete Zentrip Information

  • ACTIVE INGREDIENT

    Active ingredient (in each strip)    
    Meclizine hydrochloride 25mg


  • PURPOSE

    Purpose  
    Meclizine hydrochloride    Antiemetic


  • INDICATIONS & USAGE

    Uses
    â–  For the prevention and treatment of the nausea, vomiting, or dizziness associated with motion sickness.


  • Warnings

    Enter section text here

    Do not use in children under 12 years of age unless directed by a physician

    Ask a doctor before use if you have
    â–  glaucoma   â–  a breathing problem such as emphysema or chronic bronchitis
    â–  difficulty in urination due to enlargement of the prostate gland

    Ask a physician or pharmacist before use if you are
    â–  taking sedatives or tranquilizers

    When using this product
    â–  you may get drowsy   â–  avoid alcoholic beverages
    â–  be careful when driving a motor vehicle or operating machinery
    â–  alcohol, sedatives, and tranquilizers may increase the drowsiness effect

    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.


  • DOSAGE & ADMINISTRATION

    Directions
    To prevent motion sickness take it at least one hour before traveling    
    Adults and children 12 years of age and over:  Oral dosage is 1 to 2 strips (25 to 50 mg) to dissolve on tongue once daily, or as directed by a physician.


  • OTHER SAFETY INFORMATION

    Other information 
    â–  Store tightly closed, protected from light, at 20-30°C. (68-86°F)


  • INACTIVE INGREDIENT

    Inactive ingredients
    acesulfame potassium, , ferric oxide, hypromelloses, mannitol, menthol, orange oil, polyethylene glycol 400, sucralose, sucrose esters of fatty acids


  • PRINCIPAL DISPLAY PANEL

    zentripcart.jpg
    carton







  • PRINCIPAL DISPLAY PANEL

    zentripPDP.jpg
    PDP




  • INGREDIENTS AND APPEARANCE
    ZENTRIP 
    meclizine hydrochloride film, soluble
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49873-803
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE 25 mg
    Inactive Ingredients
    Ingredient Name Strength
    ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    MANNITOL (UNII: 3OWL53L36A)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SUCROSE STEARATE/PALMITATE ESTER (75% MONO ESTER) (UNII: L98X941W2B)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    Product Characteristics
    Color white Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49873-803-01 8 in 1 CARTON
    1 1 in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part336 02/03/2009
    Labeler - Sato Pharmaceutical Co., Ltd. (690575642)