Label: MECLIZINE HYDROCHLORIDE tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 2, 2024

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  • Drug Facts

    Active ingredient (in each tablet)
    Meclizine HCl 25 mg

  • PURPOSE

    Purpose
    Antiemetic

  • Uses

    for prevention and treatment of these symptoms associated with motion sickness:

    • nausea
    • vomiting
    • dizziness
  • WARNINGS

    Do not give to children under 12 years of age unless directed by a doctor.

    Ask a doctor before use if you have

    • a breathing problem such as emphysema or chronic bronchitis
    • glaucoma
    • trouble urinating due to an enlarged prostate gland

    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

    When using this product

    • drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery

    If pregnant or breast-feeding, ask a doctor before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

  • Directions

    • to prevent motion sickness take first dose ½ hour to 1 hour before activity
    • to treat motion sickness, take at first sign of symptoms
    • adults and children 12 years and over: 1 to 2 tablets once daily, or as directed by a doctor

  • Other information


    store in a dry place at 15° – 30°C (59° – 86°F)

  • INACTIVE INGREDIENT

    croscarmellose sodium, crospovidone, FD&C red #40 lake, french vanilla flavor, lactose, magnesium stearate, raspberry flavor, silica, sodium saccharin, stearic acid.

  • QUESTIONS

    1-800-925-4733

  • SPL UNCLASSIFIED SECTION

    Tamper Evident: Do not use if outer carton is open or if blister is open or torn.

    Important: Keep carton for future reference.

    †Our pharmacists recommend the Walgreens brand. We invite you to compare to national brands.
    ††This product is not manufactured or distributed by MedTech Products Inc., owner of the registered trademark Dramamine®.

    DISTRIBUTED BY: WALGREEN CO.
    200 WILMOT RD., DEERFIELD, IL 60015
    100% SATISFACTION GUARANTEED
    walgreens.com ©2022 Walgreen Co.
    MADE IN INDIA

  • PRINCIPAL DISPLAY PANEL

    NDC 0363-5172-07

    Compare to the active ingredient in Dramamine® All Day Less Drowsy††

    Motion Sickness Relief

    MECLIZINE HCl 25 mg / ANTIEMETIC

    All Day Relief

    Less Drowsy Formula

    Chewable

    Helps prevent nausea, dizziness & vomiting due to motion sickness

    All-day relief of motion sickness

    For adults & children 12 years & up

    Raspberry flavor

    12 Chewable Tablets

    Walgreen Label

  • INGREDIENTS AND APPEARANCE
    MECLIZINE HYDROCHLORIDE 
    meclizine hydrochloride tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5172
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    VANILLA (UNII: Q74T35078H)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    RASPBERRY (UNII: 4N14V5R27W)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    CROSPOVIDONE (UNII: 2S7830E561)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Product Characteristics
    ColorpinkScore2 pieces
    ShapeROUNDSize9mm
    FlavorVANILLA, RASPBERRYImprint Code 5172
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-5172-071 in 1 CARTON03/22/2023
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00903/22/2023
    Labeler - Walgreen Company (008965063)
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