DRAMAMINE ORIGINAL FORMULA- dimenhydrinate tablet 
Medtech Products Inc.

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Dramamine Original Formula

Drug Facts

Active ingredient

(in each tablet)

Dimenhydrinate 50 mg

Purpose

Antiemetic

Use

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

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

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

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)

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)

Revised: 12/2023
Document Id: 76ecbdd3-b960-4892-86b9-01a07390b2c7
Set id: f9302a5a-295a-4501-9332-e3f5eb387362
Version: 7
Effective Time: 20231227
 
Medtech Products Inc.