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Pill Identifier Information of Dramamine 50 MG Oral Tablet

Drug Information

Dramamine 50 MG Oral Tablet

Imprint:
Shape: C48348
Color: C48331
Ingredients: Dimenhydrinate
Size: 8.00
Score: 2
Rxtty: SY
Author: Medtech Products Inc.
Inactive Ingredients: ANHYDROUS LACTOSE / SILICON DIOXIDE / CROSCARMELLOSE SODIUM / MAGNESIUM STEARATE / CELLULOSE, MICROCRYSTALLINE>

Complete Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    (in each tablet)

    Dimenhydrinate 50 mg

  • Purpose

    Antiemetic

  • Use

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

    • nausea
    • vomiting
    • dizziness
  • Warnings

    Do not give to

    children under 2 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
    • marked drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives, and tranquilizers may increase dizziness
    • 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, the first dose should be taken ½ to 1 hour before starting activity
    • to prevent or treat motion sickness, see below:
    Adults and
    children 12
    years and over
    • take 1 to 2 tables every 4-6 hours
    • do not take more than 8 tablets in
      24 hours, or as directed by a doctor
    Children 6 to
    under 12 years
    • give ½ to 1 tablet every 6-8 hours
    • do not give more than 3 tablets in
      24 hours, or as directed by a doctor
    Children 2 to
    under 6 years
    • give ½ tablet every 6-8 hours
    • do not give more than 1 ½ tablets
      in 24 hours, or as directed by a doctor
  • Other information

    • store at room temperature 20-25ºC (68-77ºF) 
  • Inactive ingredients

    colloidal silicon dioxide, croscarmellose sodium, lactose, magnesium stearate, microcrystalline cellulose

  • Questions or comments?

    Call 1-800-382-7219

    Dramamine.com

  • PRINCIPAL DISPLAY PANEL

    Dramamine®
    motion sickness 
    Original
    Dimenhydrinate tablets/antiemetic
    12 tablets (50 mg each)

    Dramamine® motion sickness Original Dimenhydrinate tablets/antiemetic 12 tablets (50 mg each)

  • PRINCIPAL DISPLAY PANEL

    Dramamine®
    motion sickness
    Original
    Dimenhydrinate tablets/antiemetic
    36 tablets (50 mg each)

    A yellow label with a blue circle and white text AI-generated content may be incorrect.

  • INGREDIENTS AND APPEARANCE
    DRAMAMINE ORIGINAL FORMULA 
    dimenhydrinate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-901
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMENHYDRINATE (UNII: JB937PER5C) (8-CHLOROTHEOPHYLLINE - UNII:GE2UA340FM) DIMENHYDRINATE50 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColororangeScore2 pieces
    ShapeROUNDSize8mm
    FlavorORANGEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63029-901-013 in 1 BOX01/15/2012
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:63029-901-021 in 1 BOX01/15/2012
    212 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:63029-901-031 in 1 CARTON01/15/2012
    32 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00901/15/2012
    Labeler - Medtech Products Inc. (122715688)
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