DRAMAMINE- dimenhydrinate tablet, chewable 
Lil' Drug Store Products, Inc.

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Dramamine

DRUG FACTS

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 use for 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 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 accidental overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Adults and children 12 years and over
  • Take 1 to 2 chewable tablets every 4-6 hours
  • Do not take more than 8 chewable tablets in 24 hours, or as directed by a doctor
Children 6 to under 12 years
  • Give 1/2 to 1 chewable tablet every 6-8 hours
  • Do not give more than 3 chewable tablets in 24 hours, or as directed by a doctor
Children 2 to under 6 years

Give 1/2 chewable tablet every 6-8 hours

Do not give more that 1 1/2 chewable tablets in 24 hours, or as directed by a doctor

Other Information

Inactive ingredients

anhydrous citric acid, aspartame, FD&C yellow 6 aluminum lake, flavors, magnesium stearate, maltodextrin, methacrylic acid copolymer, modified starch, sorbitol

Questions?

1-800-382-7219 Dramamine.com

Dist. by Medtech Products Inc., Tarrytown, NY 10591
A Prestige Consumer Healthcare company. Made in Italy.
© 2021 Trade dress is owned by Medtech Products Inc.
All rights reserved.

PRINCIPAL DISPLAY PANEL - 50mg Tablet Pouch Blister

#1
Pharmacist
Recommended
Brand

Dimenhydrinate
Tablets/Antiemetic

Dramamine ®


motion sickness

CHEWABLE
Dual Action:

Prevents & Relieves Nausea,

Dizziness and Vomiting


4

Orange Flavored

Tablets (50 mg each)

PDP

PRINCIPAL DISPLAY PANEL - 50mg Tablet Pouch Blister

#1
Pharmacist
Recommended
Brand

Dimenhydrinate
Tablets/Antiemetic

Dramamine ®


motion sickness

CHEWABLE
Dual Action:

Prevents & Relieves Nausea,

Dizziness and Vomiting


6

Orange Flavored Tablets (50 mg each)

DRAMAMINE 6CT

PRINCIPAL DISPLAY PANEL - 50mg Tablet Pouch Box

#1
Pharmacist
Recommended
Brand

Dimenhydrinate
Tablets/Antiemetic

Dramamine ®


motion sickness

CHEWABLE
Dual Action:

Prevents & Relieves Nausea,

Dizziness and Vomiting


25 POUCHES

2 Orange Flavored Tablets (50 mg each) per Pouch

PDP

DRAMAMINE 
dimenhydrinate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-1216
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMENHYDRINATE (UNII: JB937PER5C) (CHLORTHEOPHYLLINE - UNII:GE2UA340FM) DIMENHYDRINATE50 mg
Inactive Ingredients
Ingredient NameStrength
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
SORBITOL (UNII: 506T60A25R)  
ASPARTAME (UNII: Z0H242BBR1)  
STARCH, CORN (UNII: O8232NY3SJ)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
ColororangeScore2 pieces
ShapeROUNDSize12mm
FlavorORANGEImprint Code DRA
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29485-1216-22 in 1 BLISTER PACK05/10/201012/31/2024
12 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00901/01/199412/31/2024
DRAMAMINE 
dimenhydrinate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-6925
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMENHYDRINATE (UNII: JB937PER5C) (CHLORTHEOPHYLLINE - UNII:GE2UA340FM) DIMENHYDRINATE50 mg
Inactive Ingredients
Ingredient NameStrength
ALUMINUM OXIDE (UNII: LMI26O6933)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
SORBITOL (UNII: 506T60A25R)  
ASPARTAME (UNII: Z0H242BBR1)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
ColororangeScore2 pieces
ShapeROUNDSize12mm
FlavorORANGEImprint Code DRA
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29485-6925-33 in 1 BLISTER PACK02/06/201712/31/2024
12 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00902/06/201712/31/2024
DRAMAMINE 
dimenhydrinate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-8048
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMENHYDRINATE (UNII: JB937PER5C) (CHLORTHEOPHYLLINE - UNII:GE2UA340FM) DIMENHYDRINATE50 mg
Inactive Ingredients
Ingredient NameStrength
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
SORBITOL (UNII: 506T60A25R)  
ASPARTAME (UNII: Z0H242BBR1)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
ColororangeScore2 pieces
ShapeROUNDSize12mm
FlavorORANGEImprint Code DRA
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29485-8048-225 in 1 BOX07/10/202012/31/2025
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00901/01/199412/31/2025
Labeler - Lil' Drug Store Products, Inc. (093103646)

Revised: 12/2023
Document Id: 0bc9b688-9534-6bbc-e063-6294a90ac6a7
Set id: cee22d00-e8a1-d735-e053-2995a90aec04
Version: 8
Effective Time: 20231205
 
Lil' Drug Store Products, Inc.