Label: MOTION SICKNESS RELIEF- meclizine hcl tablet

  • NDC Code(s): 41163-304-02
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 16, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active ingredient (in each tablet)

    Meclizine HCl 25 mg

  • Purpose

    Antiemetic

  • Uses

    for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness 

  • Warnings

    Do not use

    for children under 12 years of age unless directed by a doctor.

    Ask a doctor before use if you have

    • glaucoma
    • difficulty in urination due to enlargement of the prostate gland
    • a breathing problem such as emphysema or chronic bronchitis

    Ask a doctor or pharmacist before use if you are

    taking sedatives or tranquilizers.

    When using this product

    • drowsiness may occur
    • avoid alcoholic beverages
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • use caution when driving a motor vehicle or operating machinery 

    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.

  • Directions

    • do not take more than directed
    • take first dose 1/2 to 1 hour before starting activity
    • adults and children 12 years and over: 1 to 2 tablets once daily, or as directed by a doctor
  • Other information

    • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
    • protect from heat and humidity
    • use by expiration date on package
  • Inactive ingredients

    colloidal silicon dioxide, D&C yellow #10 aluminum lake, lactose monohydrate, magnesium stearate, pregelatinized starch

  • Questions or comments?

    1-855-423-2630

  • Principal Display Panel

    EQUALINE®

    compare to Dramamine®
    Less Drowsy
    active ingredient*
    NDC 41163-304-02

    motion sickness relief
    meclizine HCl 25 mg
    (antiemetic)

    less drowsy formula

    Ages 12 Years & Over
    helps prevent nausea & dizziness
    due to motion sickness
    for up to 24 hours

    12 tablets 

    TAMPER EVIDENT:
    USE ONLY IF THIS BLISTER IS INTACT

    actual size

    *This product is not manufactured or distributed by
    Medtech Products Inc., owner of the registered
    trademark Dramamine® Less Drowsy.
    50844 ORG042340302

    100% Quality
    GUARANTEED

    DISTRIBUTED BY UNFI
    PROVIDENCE, RI 02908 USA
    855-423-2630

    Equaline 44-403

    Equaline 44-403

  • INGREDIENTS AND APPEARANCE
    MOTION SICKNESS RELIEF 
    meclizine hcl tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-304
    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)  
    D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColoryellowScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code 44;403
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-304-021 in 1 PACKAGE06/24/2002
    112 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00906/24/2002
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.038154464pack(41163-304)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867837manufacture(41163-304) , pack(41163-304)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305pack(41163-304)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.117025878manufacture(41163-304)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!