DRAMAMINE LESS DROWSY- meclizine hydrochloride tablet 
Medtech Products Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Dramamine Less Drowsy

Drug Facts

Active ingredient

(in each tablet)

Meclizine HCI 25 mg

Purpose

Antiemetic

Use

for prevention and treatment of these symptoms 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

  • 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) right away.

Directions

Other information

Inactive ingredients

corn starch, colloidal silicon dioxide, D&C yellow no. 10 aluminum lake, lactose, magnesium stearate, microcrystalline cellulose

Questions?

1-800-382-7219

PRINCIPAL DISPLAY PANEL

All Day LESS DROWSY
Dramamine®
Meclizine hydrochloride tablets/Antiemetic


8 TABLETS (25 mg EACH)

PRINCIPAL DISPLAY PANEL
All Day LESS DROWSY 
Dramamine®
Meclizine hydrochloride tablets/Antiemetic 

8 TABLETS (25 mg EACH)

DRAMAMINE LESS DROWSY 
meclizine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-903
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
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
STARCH, CORN (UNII: O8232NY3SJ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
Product Characteristics
ColorYELLOWScore2 pieces
ShapeROUNDSize9mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-903-011 in 1 BLISTER PACK09/01/2011
18 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33609/01/2011
Labeler - Medtech Products Inc. (122715688)

Revised: 2/2019
Document Id: f8950127-9e99-4891-9a4d-5967dcb31137
Set id: fa6a0969-7427-4b87-bc04-a2792665c218
Version: 3
Effective Time: 20190219
 
Medtech Products Inc.